Diabetic NeuropathyPINSNCT02672059
Pain In Neuropathy Study
An observational study of Diabetic Neuropathy and Neuropathic Pain, run by King's College London at 1 site in United Kingdom.
Trial summary
In the context of peripheral neuropathy, we will aim to elucidate correlates between sensory symptoms and: Sensory nerve dysfunction. Cutaneous small nerve fibre innervation density. Psychological co-morbidity. Circadian rhythm disturbance co-morbidity. Functionality and Quality of life. Read more about this study
- Who is it for?
- Ages 18 to 99 yearsHealthy volunteers can take part
- Conditions the study is for
- Diabetic Neuropathy, Neuropathic Pain, Chronic Pain
- What is being tested?
- Observation
- How many people
- 700 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- Feb 2011to Jun 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 99 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Subjects with peripheral neuropathies associated with diabetes, carpal tunnel syndrome or others.
Who may be able to join
- Patients who are ≥18 years of age who have a diagnosis of peripheral neuropathy based on a prior clinical assessment combined with supportive clinical investigations such as abnormal nerve conduction studies, reduced intraepidermal nerve or abnormal findings on quantitative sensory testing.
- If supportive clinical investigations (as described above) are not available at entry into the study a neuropathy disability scale ≥3 (Pham et al., 2000).
- And patients with symptoms highly suggestive of neuropathy that in the judgement of the clinical researcher are suitable for the study even if they do not fulfill other inclusion criteria.
- Patients who do not fulfill any of the exclusion criteria.
Who cannot join
- Subjects who are pregnant.
- Subjects with insufficient command of English to obtain consent from or to complete the study questionnaires.
- Subjects with insufficient mental capacity to obtain consent from or complete study questionnaires.
- Subjects with concurrent severe psychological or psychiatric disorders.
- Patients with moderate to severe pain form other causes that may confound assessment or reporting of pain (eg. spinal canal stenosis).
- Patients with central nervous lesions, which may complicate somatosensory testing.
- Who is in the opinion of the investigator unsuitable for participation in the study.
- Skin biopsies will not be conducted on patients that are anticoagulated or who have any other contra-indication to skin biopsy (if patients decline a skin biopsy they will NOT be excluded from the study).
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site, 1 recruiting
- Recruiting
Nuffield Department of Clinical Neurosciences
Oxford, Oxfordshire, OX3 9DU
Andreas Themistocleous, PhD, +44 1865234543, andreas.themistocleous@ndcn.ox.ac.uk
Mathilde Pascal, +44 1865223374, mathilde.pascal@ndcn.ox.ac.uk
About this study
In the context of peripheral neuropathy, we will aim to elucidate correlates between sensory symptoms and:
- Sensory nerve dysfunction.
- Cutaneous small nerve fibre innervation density.
- Psychological co-morbidity.
- Circadian rhythm disturbance co-morbidity.
- Functionality and Quality of life.
- Patterns of human brain activity in a subset of patients that consent to participate in the FMRI (functional magnetic resonance imaging) component of PINS.
- We will also collect blood samples in this phenotyped cohort of patients. These blood samples coupled with detailed phenotype data will investigate potential gene associations only in the development of painful neuropathy.
- Knowledge gained from the study will be used to aid the further development of pain questionnaires, designed to detect patients with painful neuropathy. 4.Knowledge gained from the study will be invaluable in informing on-going investigations of painful peripheral neuropathy in animal models, both in our laboratory and others.
Read the detailed description
Very little is currently known about why some patients with peripheral neuropathy develop neuropathic pain, whilst others do not. It is anticipated that this study will begin to identify features of the peripheral neuropathy, which are and are not, associated with the development and intensity of neuropathic pain and therefore begin to elucidate factors, which underlie pain. We will also compare findings in neuropathies resulting from diverse aetiologies including diabetes, HIV and idiopathic axonal neuropathies in order to investigate, whether there are differences in pain symptomatology, NCS, QST, patterns of evoked brain activity and small fibre dysfunction in these different contexts.
We would like to answer the following question:
'In patients suffering from peripheral neuropathy what are the relationships between pain symptomatology and peripheral sensory dysfunction, intraepidermal nerve fibre density (IENFD) and psychological, and circadian rhythm co-morbidity as well as in everyday functionality?
1.2.1 Quantitative sensory testing (QST) and neuropathic pain.
Nerve conduction studies (NCS) predominantly assess large fibre function and indeed in the context of small fibre neuropathy are often normal. We propose to assess the utility of two relatively non-invasive tools, which are routinely used, both in our practice and elsewhere, to assess small fibre dysfunction: quantitative sensory testing (QST) and intraepidermal nerve fibre density (IENFD). There have been studies examining both of these in the context of neuropathy, but the exact relationship of these measures to abnormalities to pain, quality of life and psychological state is largely unknown.
QST is a method for accurately determining sensory thresholds in human skin and is particularly useful for determining dysfunction in the nociceptive smaller diameter nerve fibres, although the precise utility of QST in routine clinical neuropathic pain management perhaps requires some further evaluation. There is also increasing interest in using QST in combination with assessment of pain descriptors to give insights into the underlying pathophysiological mechanisms of chronic pain. For example, the presence of brush evoked dynamic allodynia indicates sensitisation at the spinal level. Although QST is widely used as an assessment tool for small fibre function and sensory phenotype in neuropathies associated with pain often only certain individual components have been measured (e.g. thermal and vibration thresholds as opposed to the full battery of tests required to give the complete sensory assessment). Previous studies have also suggested that patients with painful neuropathy may also display hyperalgesia to mechanical and thermal suprathreshold stimuli, however these studies have contained relatively small numbers of subjects. We will therefore further characterise this phenomenon by conducting additional suprathreshold mechanical and thermal stimuli according to a method previously described, in addition to the standard German Neuropathic Pain Network QST protocol, and also we will include variations in ambient temperature (in the range of 10 to 35 °C) to assess if characteristics related to the sensory testing eventually change.
1.2.2 Intra-epidermal nerve fibre density (IENFD) and neuropathic pain.
Measurement of IENFD is a relatively simple assay which can be performed in relatively innocuous 3mm punch biopsies of skin, a routine dermatological investigation. Its utility in the assessment of small fibre function in peripheral neuropathies is clear. Peripheral neuropathies of diverse aetiologies are associated with reduced epidermal innervation density however the exact relationship of this reduction to pain and pain co-morbidities requires proper evaluation. Residual skin tissue will be stored in compliance with The Human Tissue Act, for further biochemical analysis.
1.2.3 Nerve Conduction Studies Axon Reflex and Neuropathic Pain Characteristically, different types of peripheral neuropathy exhibit patterns of demyelination or axonopathy in large fibres. The rationale for the procedure in this study is to discard other pathologies that may account as the main etiology causing pain in the context of a peripheral neuropathy. Guillain-Barre Syndrome, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Vasculitic Neuropathies and others can account for both neuropathy and pain allowing us to make the sample more homogeneous. Nerve conduction studies are usually safe procedures in which the indemnity of the axon and its myelin sheath are tested using external electrical stimuli. As a part of the protocol we have these tests . As a part of the study, Electromyography (EMG) will not be included either.
If NCS have been performed as part of the patients routine medical care these results will be recorded.
As a further means of assessing the physiological integrity of C fibers in patients suffering from carpal tunnel syndrome we will elicit an axon reflex. This reflex involves the transcutaneous application of agents such as histamine via iontophoresis (electrical current). The histamine will stimulate the peripheral nerve endings of the small diameter C fibres. Their stimulation induces a vasodilatation, which is visible as a flare response of the skin. The evaluation of the extent of the flare response is used as an indication of the integrity of the small diameter C fibre population.
1.2.4 Psychological co-morbidity, quality of life and neuropathic pain
Whilst some studies have examined aspects of pain in the context of peripheral neuropathy, these do not go beyond more than simple measurement of pain intensity or sensory characteristics and there is only a limited literature which has explored the interactions between pain, psychological status and quality of life. Neuropathic pain in general is associated with multiple psychological problems which impact upon quality of life. These include circadian rhythm disturbances (e.g. sleeping difficulty: moderate to severe in 60% of patients), lack of energy (55%), drowsiness (39%) and difficulty in concentration (36%); similar findings have been specifically documented in diabetic neuropathy. Severe to moderate depression and anxiety also occur in about 30% of neuropathic pain patients. In general, beliefs and fears concerning the pain and its implications contribute substantially to determining mood and behaviour. Since neuropathic pain is relatively common in the context of peripheral neuropathy the question arises as to what extent pain is the driver of these co-morbidities - the answer to this is not known, but large randomised controlled trials of analgesic interventions in neuropathic pain states indicate that as pain intensity reduces so does the severity of these co-morbidities. To answer this question we will first need to identify specific tools for the measurement of neuropathic pain co-morbidity in the context of peripheral neuropathy this is one of the aims of this proposal and we will evaluate a variety of existing assessment tools. Another issue is that it is likely that psychological co-morbidity influences the self reporting of pain intensity, which is a usual primary outcome measure in clinical trials of neuropathic pain analgesic agents.
We will use a battery of psychological instruments to determine the psychological and quality of life in those subjects with peripheral neuropathy and identify differences between those who do and do not suffer from neuropathic pain.
We will also attempt to further validate a number of neuropathy screening and assessment tools; the Brief Peripheral Neuropathy Screen (BPNS) and the Utah Early Neuropathy Scale (UENS). The BPNS and UENS tools has been previously evaluated in the context of HIV and diabetic neuropathy respectively, however our study would provide additional invaluable information in the light of both QST and IENFD findings in the context of axonal polyneuropathy resulting from diverse aetiologies.
1.2.4 Blood samples
We will collect blood samples (30mls) from each subject, which will be stored at -80C in a locked freezer. This coupled with the detailed phenotype data collected, will inform studies investigating potential genetic associations in the development of neuropathic pain. A serum sample will also be stored for the consideration of future biomarker studies.
1.2.5 Imaging human brain activity in a subset of PINS participants
The advent of functional imaging techniques allowed researchers to begin to look within the human brain to observe what pain looks like in the brain. Initially, pain imaging research determined that pain is not processed by a single brain region but instead engages several distributed cortical areas. The group of brain regions that are most active during pain are commonly referred to as the 'pain matrix'. This includes: primary and secondary somatosensory cortices (SI, SII), insular, anterior cingulate, and prefrontal cortices and the thalamus. However, pain is not purely a sensory event but is also reflective of how the person feels about their pain. Factors that vary widely across a population such as memories, emotion, pathology, genetics, and cognitive factors all directly affect how an individual experiences pain. Because of this, the pain matrix provides an incomplete picture of what is happening in the brain during pain. Pain imaging studies have begun to validate this perspective. For example, Derbyshire et al. showed activation of the key pain matrix regions even when subjects were not in pain. From a study looking at chronic pain sufferers, Baliki et al. showed that a series of other key brain regions were active that were outside the pain matrix. It is essential for brain imaging research to update the notion of the 'pain matrix' to account for these inconsistencies. Therefore, in this study we would like to see which areas of the brain are activated when the peripheral markers of the polyneuropathy are targeted by a range of noxious and non-noxious stimulations, so that we can determine the key brain regions involved in pain processing.
- Conditions
- Diabetic Neuropathy, Neuropathic Pain, Chronic Pain, Carpal Tunnel Syndrome, Peripheral Neuropathies
- Being tested
- Observation
- Medical subject headings
- Diabetic Neuropathies, Neuralgia, Chronic Pain, Carpal Tunnel Syndrome, Peripheral Nervous System Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ObservationOther
No intervention
| Study group | Role | What they receive |
|---|---|---|
| Peripheral Neuropathy | Patients with peripheral neuropathy (observational study, no interventions) Receives: Other: Observation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Diagnosis of neuropathy
Toronto Clinical Scoring System of 4
Measured: Day 1
Secondary outcomes (14)
Demographics
Main demographic visits
Measured: Day 1
Detailed medical history
Past clinical records of patients relevant to the current disease status
Measured: Day 1
7-days pain diary
Patients will have 7-days pain diaries with a numeric rating scale from 0 to 10
Measured: Day 1
Pain related anxiety
Patients will answer the Pain Anxiety Symptoms Scale (PASS-20)
Measured: Day 1
Measures of quality of life
Patients will answer the 36-Item Short Form Survey -quality of life questionnaire-
Measured: Day 1
Measures of sleep interference
Sleep quality is assessed through the use of questionnaires
Measured: Day 1
Nerve Conduction Studies
Neurophysiology will be conducted to assess nerve integrity
Measured: Day 1
Sensory Thermal Thresholds
Thermal thresholds will be measured in degrees centigrade
Measured: Day 1
Sensory Mechanical Detection Thresholds
Mechanical Detection Thresholds will be measured in millinewtons
Measured: Day 1
Intra-Epidermal Nerve Fibre density
Measurement of nerve fibres in the skin of patients - leg or finger-
Measured: Day 1
Blood samples - DNA
Blood samples coupled with detailed phenotype data will investigate potential gene associations in the development of painful neuropathy
Measured: Within 6 months of visit
Blood samples - RNA
Blood samples coupled with detailed phenotype data will investigate potential blood markers associations in the development of painful neuropathy
Measured: Within 18 months of visit
Blood samples - Serum
Blood samples coupled with detailed phenotype data will investigate potential blood markers associations only in the development of painful neuropathy
Measured: Within 18 months of visit
Synovium tissue collection for RNA
Synovium from around the nerve and tendons coupled with detailed phenotype data will investigate potential blood markers associations only in the development of painful neuropathy
Measured: Within 18 months of visit
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Feb 2016 (estimated)
- Study startFeb 2011
- Primary completionJun 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Diabetic NeuropathyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 700 participants (estimated)
Sponsor and investigators
- Lead sponsor
- King's College London
- Sponsor type
- University, hospital or other
- Collaborators
- University of Oxford, Imperial College London, Sheffield Teaching Hospitals NHS Foundation Trust
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02672059
- Sponsor's protocol ID
- 10/H0706/035
- Other IDs
- 9755
- Acronym
- PINS
- Status last verified
- Sep 2019
- First submitted
- 5 Jan 2016
- Last updated
- 17 Sep 2019
- Results posted
- No
- Data monitoring committee
- No
Publications
Phillips TJC, Brown M, Ramirez JD, Perkins J, Woldeamanuel YW, Williams ACC, Orengo C, Bennett DLH, Bodi I, Cox S, Maier C, Krumova EK, Rice ASC. Sensory, psychological, and metabolic dysfunction in HIV-associated peripheral neuropathy: A cross-sectional deep profiling study. Pain. 2014 Sep;155(9):1846-1860. doi: 10.1016/j.pain.2014.06.014. Epub 2014 Jun 26.
PubMed 24973717Schmid AB, Bland JD, Bhat MA, Bennett DL. The relationship of nerve fibre pathology to sensory function in entrapment neuropathy. Brain. 2014 Dec;137(Pt 12):3186-99. doi: 10.1093/brain/awu288. Epub 2014 Oct 27.
PubMed 25348629Ramirez JD, Barnes PRJ, Mills KR, Bennett DLH. Intermediate Charcot-Marie-Tooth disease due to a novel Trp101Stop myelin protein zero mutation associated with debilitating neuropathic pain. Pain. 2012 Aug;153(8):1763-1768. doi: 10.1016/j.pain.2012.05.015. Epub 2012 Jun 16.
PubMed 22704856Segerdahl AR, Xie J, Paterson K, Ramirez JD, Tracey I, Bennett DLH. Imaging the neural correlates of neuropathic pain and pleasurable relief associated with inherited erythromelalgia in a single subject with quantitative arterial spin labelling. Pain. 2012 May;153(5):1122-1127. doi: 10.1016/j.pain.2011.12.012. Epub 2012 Feb 24.
PubMed 22365309
Study at a glance
From the registry record, last updated by the sponsor on 17 Sep 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pain In Neuropathy Study
- ClinicalTrials.gov ID
- NCT02672059
- Acronym / sponsor ID
- PINS / 10/H0706/035
- Conditions
- Diabetic Neuropathy, Neuropathic Pain, Chronic Pain, Carpal Tunnel Syndrome, Peripheral Neuropathies
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 700 participants (estimated)
- Lead sponsor
- King's College LondonUniversity, hospital or other
- Collaborators
- University of Oxford, Imperial College London, Sheffield Teaching Hospitals NHS Foundation Trust
- Study start
- Feb 2011
- Primary completion
- Jun 2021 (estimated)
- First posted
- 3 Feb 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
In the context of peripheral neuropathy, we will aim to elucidate correlates between sensory symptoms and:
- Sensory nerve dysfunction.
- Cutaneous small nerve fibre innervation density.
- Psychological co-morbidity.
- Circadian rhythm disturbance co-morbidity.
- Functionality and Quality of life.
- Patterns of human brain activity in a subset of patients that consent to participate in the FMRI (functional magnetic resonance imaging) component of PINS.
- We will also collect blood samples in this phenotyped cohort of patients. These blood samples coupled with detailed phenotype data will investigate potential gene associations only in the development of painful neuropathy.
- Knowledge gained from the study will be used to aid the further development of pain questionnaires, designed to detect patients with painful neuropathy. 4.Knowledge gained from the study will be invaluable in informing on-going investigations of painful peripheral neuropathy in animal models, both in our laboratory and others.
Detailed description
Very little is currently known about why some patients with peripheral neuropathy develop neuropathic pain, whilst others do not. It is anticipated that this study will begin to identify features of the peripheral neuropathy, which are and are not, associated with the development and intensity of neuropathic pain and therefore begin to elucidate factors, which underlie pain. We will also compare findings in neuropathies resulting from diverse aetiologies including diabetes, HIV and idiopathic axonal neuropathies in order to investigate, whether there are differences in pain symptomatology, NCS, QST, patterns of evoked brain activity and small fibre dysfunction in these different contexts.
We would like to answer the following question:
'In patients suffering from peripheral neuropathy what are the relationships between pain symptomatology and peripheral sensory dysfunction, intraepidermal nerve fibre density (IENFD) and psychological, and circadian rhythm co-morbidity as well as in everyday functionality?
1.2.1 Quantitative sensory testing (QST) and neuropathic pain.
Nerve conduction studies (NCS) predominantly assess large fibre function and indeed in the context of small fibre neuropathy are often normal. We propose to assess the utility of two relatively non-invasive tools, which are routinely used, both in our practice and elsewhere, to assess small fibre dysfunction: quantitative sensory testing (QST) and intraepidermal nerve fibre density (IENFD). There have been studies examining both of these in the context of neuropathy, but the exact relationship of these measures to abnormalities to pain, quality of life and psychological state is largely unknown.
QST is a method for accurately determining sensory thresholds in human skin and is particularly useful for determining dysfunction in the nociceptive smaller diameter nerve fibres, although the precise utility of QST in routine clinical neuropathic pain management perhaps requires some further evaluation. There is also increasing interest in using QST in combination with assessment of pain descriptors to give insights into the underlying pathophysiological mechanisms of chronic pain. For example, the presence of brush evoked dynamic allodynia indicates sensitisation at the spinal level. Although QST is widely used as an assessment tool for small fibre function and sensory phenotype in neuropathies associated with pain often only certain individual components have been measured (e.g. thermal and vibration thresholds as opposed to the full battery of tests required to give the complete sensory assessment). Previous studies have also suggested that patients with painful neuropathy may also display hyperalgesia to mechanical and thermal suprathreshold stimuli, however these studies have contained relatively small numbers of subjects. We will therefore further characterise this phenomenon by conducting additional suprathreshold mechanical and thermal stimuli according to a method previously described, in addition to the standard German Neuropathic Pain Network QST protocol, and also we will include variations in ambient temperature (in the range of 10 to 35 °C) to assess if characteristics related to the sensory testing eventually change.
1.2.2 Intra-epidermal nerve fibre density (IENFD) and neuropathic pain.
Measurement of IENFD is a relatively simple assay which can be performed in relatively innocuous 3mm punch biopsies of skin, a routine dermatological investigation. Its utility in the assessment of small fibre function in peripheral neuropathies is clear. Peripheral neuropathies of diverse aetiologies are associated with reduced epidermal innervation density however the exact relationship of this reduction to pain and pain co-morbidities requires proper evaluation. Residual skin tissue will be stored in compliance with The Human Tissue Act, for further biochemical analysis.
1.2.3 Nerve Conduction Studies Axon Reflex and Neuropathic Pain Characteristically, different types of peripheral neuropathy exhibit patterns of demyelination or axonopathy in large fibres. The rationale for the procedure in this study is to discard other pathologies that may account as the main etiology causing pain in the context of a peripheral neuropathy. Guillain-Barre Syndrome, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Vasculitic Neuropathies and others can account for both neuropathy and pain allowing us to make the sample more homogeneous. Nerve conduction studies are usually safe procedures in which the indemnity of the axon and its myelin sheath are tested using external electrical stimuli. As a part of the protocol we have these tests . As a part of the study, Electromyography (EMG) will not be included either.
If NCS have been performed as part of the patients routine medical care these results will be recorded.
As a further means of assessing the physiological integrity of C fibers in patients suffering from carpal tunnel syndrome we will elicit an axon reflex. This reflex involves the transcutaneous application of agents such as histamine via iontophoresis (electrical current). The histamine will stimulate the peripheral nerve endings of the small diameter C fibres. Their stimulation induces a vasodilatation, which is visible as a flare response of the skin. The evaluation of the extent of the flare response is used as an indication of the integrity of the small diameter C fibre population.
1.2.4 Psychological co-morbidity, quality of life and neuropathic pain
Whilst some studies have examined aspects of pain in the context of peripheral neuropathy, these do not go beyond more than simple measurement of pain intensity or sensory characteristics and there is only a limited literature which has explored the interactions between pain, psychological status and quality of life. Neuropathic pain in general is associated with multiple psychological problems which impact upon quality of life. These include circadian rhythm disturbances (e.g. sleeping difficulty: moderate to severe in 60% of patients), lack of energy (55%), drowsiness (39%) and difficulty in concentration (36%); similar findings have been specifically documented in diabetic neuropathy. Severe to moderate depression and anxiety also occur in about 30% of neuropathic pain patients. In general, beliefs and fears concerning the pain and its implications contribute substantially to determining mood and behaviour. Since neuropathic pain is relatively common in the context of peripheral neuropathy the question arises as to what extent pain is the driver of these co-morbidities - the answer to this is not known, but large randomised controlled trials of analgesic interventions in neuropathic pain states indicate that as pain intensity reduces so does the severity of these co-morbidities. To answer this question we will first need to identify specific tools for the measurement of neuropathic pain co-morbidity in the context of peripheral neuropathy this is one of the aims of this proposal and we will evaluate a variety of existing assessment tools. Another issue is that it is likely that psychological co-morbidity influences the self reporting of pain intensity, which is a usual primary outcome measure in clinical trials of neuropathic pain analgesic agents.
We will use a battery of psychological instruments to determine the psychological and quality of life in those subjects with peripheral neuropathy and identify differences between those who do and do not suffer from neuropathic pain.
We will also attempt to further validate a number of neuropathy screening and assessment tools; the Brief Peripheral Neuropathy Screen (BPNS) and the Utah Early Neuropathy Scale (UENS). The BPNS and UENS tools has been previously evaluated in the context of HIV and diabetic neuropathy respectively, however our study would provide additional invaluable information in the light of both QST and IENFD findings in the context of axonal polyneuropathy resulting from diverse aetiologies.
1.2.4 Blood samples
We will collect blood samples (30mls) from each subject, which will be stored at -80C in a locked freezer. This coupled with the detailed phenotype data collected, will inform studies investigating potential genetic associations in the development of neuropathic pain. A serum sample will also be stored for the consideration of future biomarker studies.
1.2.5 Imaging human brain activity in a subset of PINS participants
The advent of functional imaging techniques allowed researchers to begin to look within the human brain to observe what pain looks like in the brain. Initially, pain imaging research determined that pain is not processed by a single brain region but instead engages several distributed cortical areas. The group of brain regions that are most active during pain are commonly referred to as the 'pain matrix'. This includes: primary and secondary somatosensory cortices (SI, SII), insular, anterior cingulate, and prefrontal cortices and the thalamus. However, pain is not purely a sensory event but is also reflective of how the person feels about their pain. Factors that vary widely across a population such as memories, emotion, pathology, genetics, and cognitive factors all directly affect how an individual experiences pain. Because of this, the pain matrix provides an incomplete picture of what is happening in the brain during pain. Pain imaging studies have begun to validate this perspective. For example, Derbyshire et al. showed activation of the key pain matrix regions even when subjects were not in pain. From a study looking at chronic pain sufferers, Baliki et al. showed that a series of other key brain regions were active that were outside the pain matrix. It is essential for brain imaging research to update the notion of the 'pain matrix' to account for these inconsistencies. Therefore, in this study we would like to see which areas of the brain are activated when the peripheral markers of the polyneuropathy are targeted by a range of noxious and non-noxious stimulations, so that we can determine the key brain regions involved in pain processing.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Peripheral Neuropathy | – | Other: ObservationPatients with peripheral neuropathy (observational study, no interventions) |
Who may qualify
- Ages
- 18 to 99 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Subjects with peripheral neuropathies associated with diabetes, carpal tunnel syndrome or others.
Key inclusion criteria (4 listed)
- Patients who are ≥18 years of age who have a diagnosis of peripheral neuropathy based on a prior clinical assessment combined with supportive clinical investigations such as abnormal nerve conduction studies, reduced intraepidermal nerve or abnormal findings on quantitative sensory testing.
- If supportive clinical investigations (as described above) are not available at entry into the study a neuropathy disability scale ≥3 (Pham et al., 2000).
- And patients with symptoms highly suggestive of neuropathy that in the judgement of the clinical researcher are suitable for the study even if they do not fulfill other inclusion criteria.
- Patients who do not fulfill any of the exclusion criteria.
Key exclusion criteria (8 listed)
- Subjects who are pregnant.
- Subjects with insufficient command of English to obtain consent from or to complete the study questionnaires.
- Subjects with insufficient mental capacity to obtain consent from or complete study questionnaires.
- Subjects with concurrent severe psychological or psychiatric disorders.
- Patients with moderate to severe pain form other causes that may confound assessment or reporting of pain (eg. spinal canal stenosis).
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ObservationNo intervention | Other | Peripheral Neuropathy |
Primary outcome
Diagnosis of neuropathy
Time frame: Day 1
Toronto Clinical Scoring System of 4
14 secondary outcomes
Demographics
Time frame: Day 1
Detailed medical history
Time frame: Day 1
7-days pain diary
Time frame: Day 1
Pain related anxiety
Time frame: Day 1
Measures of quality of life
Time frame: Day 1
Measures of sleep interference
Time frame: Day 1
Nerve Conduction Studies
Time frame: Day 1
Sensory Thermal Thresholds
Time frame: Day 1
Sensory Mechanical Detection Thresholds
Time frame: Day 1
Intra-Epidermal Nerve Fibre density
Time frame: Day 1
Blood samples - DNA
Time frame: Within 6 months of visit
Blood samples - RNA
Time frame: Within 18 months of visit
Blood samples - Serum
Time frame: Within 18 months of visit
Synovium tissue collection for RNA
Time frame: Within 18 months of visit
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Sep 2019.
- Background: PubMed 24973717Phillips TJC, Brown M, Ramirez JD, Perkins J, Woldeamanuel YW, Williams ACC, Orengo C, Bennett DLH, Bodi I, Cox S, Maier C, Krumova EK, Rice ASC. Sensory, psychological, and metabolic dysfunction in HIV-associated peripheral neuropathy: A cross-sectional deep profiling study. Pain. 2014 Sep;155(9):1846-1860. doi: 10.1016/j.pain.2014.06.014. Epub 2014 Jun 26.
- Results publication: PubMed 25348629Schmid AB, Bland JD, Bhat MA, Bennett DL. The relationship of nerve fibre pathology to sensory function in entrapment neuropathy. Brain. 2014 Dec;137(Pt 12):3186-99. doi: 10.1093/brain/awu288. Epub 2014 Oct 27.
- Results publication: PubMed 22704856Ramirez JD, Barnes PRJ, Mills KR, Bennett DLH. Intermediate Charcot-Marie-Tooth disease due to a novel Trp101Stop myelin protein zero mutation associated with debilitating neuropathic pain. Pain. 2012 Aug;153(8):1763-1768. doi: 10.1016/j.pain.2012.05.015. Epub 2012 Jun 16.
- Results publication: PubMed 22365309Segerdahl AR, Xie J, Paterson K, Ramirez JD, Tracey I, Bennett DLH. Imaging the neural correlates of neuropathic pain and pleasurable relief associated with inherited erythromelalgia in a single subject with quantitative arterial spin labelling. Pain. 2012 May;153(5):1122-1127. doi: 10.1016/j.pain.2011.12.012. Epub 2012 Feb 24.
- A team at the University of Oxford would like to recruit people aged over 18 who have diabetes and neuropathy to a study of the causes of neuropathic pain. Their findings could inform the development of new therapies. (Recruiting until June 2017)Link provided by the sponsor.
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Lower Extremity Amputee, Diabetic Peripheral Neuropathy
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Nuffield Department of Clinical Neurosciences
Oxford, United Kingdom
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Diabetic Neuropathy and Neuropathic Pain, run by King's College London at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 17 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Diagnosis of neuropathy (time frame: Day 1). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02672059, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Sep 2019.