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NeuropathologyNEUROBISITENCT02767583

Assessment of the Prevalence of Small Fiber Peripheral Neuropathy Among Non-diabetic Obese Patients

A study testing Exams in people with Neuropathology, run by Fondation Hôpital Saint-Joseph at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Background / rational: Obesity is associated with significant comorbidities including type 2 diabetes (insulin resistance), heart disease, stroke, hypertension, sleep apnea syndrome, dyslipidemia, cancer, hepatobiliary diseases, orthopedic complications and psychosocial impact 1 . Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Neuropathology
What is being tested?
Exams
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
16 participants
Where
1 siteFrance
Study dates
2 Mar 2015to 30 Jun 2017
Phase
Interventional
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 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • morbidly obese patients:
  • BMI 35-55 kg / m²
  • Male or female
  • Age> 18 and <60 years
  • Consultant for the first time at the Centre of obesity of Paris Saint Joseph Hospital Group.

Who cannot join

  • Diabetes known treaty
  • Co-morbidity related to obesity: heart disease, respiratory failure
  • Other causes of peripheral neuropathy:
  • Alcohol Poisoning
  • Renal failure (clearance ≤ 60 mL / min)
  • Infection HIV, hepatitis B, C
Show all 14Show fewer
  • Deficiencies vitamins B1, B6, B12, folate
  • Treatment with vitamin B6
  • thyroid disease antecedent
  • Previous history of autoimmune disease
  • Previous history of cancer
  • Previous history of neurotoxic treatment (chemotherapy, etc. see list provided in annex)
  • ICU hospitalization antecedent> 48 hours.
  • known history of peripheral neuropathy.

Trial locations and contacts

1 site in 1 country.

France1 site
  • Groupe Hopitalier Paris Saint Joseph Service de neurologie

    Paris, Île-de-France Region, 75014

Other trials in France

About this study

Background / rational:

Obesity is associated with significant comorbidities including type 2 diabetes (insulin resistance), heart disease, stroke, hypertension, sleep apnea syndrome, dyslipidemia, cancer, hepatobiliary diseases, orthopedic complications and psychosocial impact 1 .

Read more

Peripheral neuropathy is a known complication in the type I and II diabetes and glucose intolerance and metabolic syndrome in 2. Outside of diabetes (type I and II) that are associated with cardiovascular risk high vascular, presence of metabolic syndrome constitutes in itself a well demonstrated vascular risk factor. Its definition requires the presence of three elements from the following 5: abdominal obesity (high waist circumference), high blood pressure, high fasting blood sugar, high triglycerides and / low HDL-cholesterol 3.

This peripheral neuropathy predominantly affects sensory fibers of small poorly myelinated diameter (Aδ fibers and C) and autonomous sensory fibers and is called small fiber neuropathy 4. The cardinal sign of NAION is the presence of neuropathic pain but abnormalities in physical examination are often absent and conventional electromyography is faulted to make the diagnosis. These small fibers are also constituent of the autonomic nervous system and causes damage autonomic dysfunction that can manifest the cardiovascular system (hypotension, cardiac conduction disorders), digestive, sweat, sphincter. neuropathy of the diagnosis of small fibers is suggested clinically by the presence of neuropathic pain often contrasting with a normal clinical examination. The confirmation is based on electrophysiology with various techniques and quantification of intra-epidermal nerve fibers.

Main objective / secondary:

Primary objective :

To determine the prevalence of a small fiber peripheral neuropathy in nondiabetic obese patients, by measuring skin conductance ion Chlorine (Sudoscan®) evaluating small fibers C autonomic

Secondary objectives:

  • Evaluation of the prevalence of occurrence of peripheral neuropathy by Sudoscan® during follow-up after treatment of obese patients with bariatric surgery (months) M1, 3, 6, 9, 12.
  • Correlation of results obtained Sudoscan® quantitative sensory testing (QST) Thermotest® evaluating small sensory fibers Aδ, among non-operated non-diabetic obese patients and in the postoperative follow-up (months) M1, 3, 6, 9, 12.
  • Characterization of electromyographic parameters (motor and sensory conduction) in patients with a skin conductance measured by lowered Sudoscan® and / or a threshold of sensitivity to pain increased Thermotest®.
  • Correlation between the presence of a small fiber neuropathy in non-diabetic obese subjects with clinical and biological parameters collected.

Methodology Design: prospective, single-center Study duration: 24 months (estimate: 3-5 patients included / week of 15 patients collected in central obesity / week) including 12 months of inclusion.

Number of topics to include: 100 over a period of one year to adjust to the rhythm of the inclusions.

As mentioned, patients will be a measure of impedance of the skin to products chlorine ions by the sweat glands via the Sudoscan®, marketed and used among diabetic patients or not for the detection of violations neuropathic (cf. references and CE certificate attached to the dossier).

The Thermotest® is also marketed and used in diabetic and non-diabetic patients (see references and CE certificate attached to the dossier).

Our center has gained experience of these techniques for the detection of peripheral neuropathy in several patient populations (diabetes and cancer in particular); manipulators (doctors and technicians) are trained in these techniques.

Read the detailed description

Main objective / secondary:

Primary objective :

To determine the prevalence of a small fiber peripheral neuropathy in nondiabetic obese patients, by measuring skin conductance ion Chlorine (Sudoscan®) evaluating small fibers C autonomic

Secondary objectives:

  • Evaluation of the prevalence of occurrence of peripheral neuropathy by Sudoscan® during follow-up after treatment of obese patients with bariatric surgery (months) M1, 3, 6, 9, 12.
  • Correlation of results obtained Sudoscan® quantitative sensory testing (QST) Thermotest® evaluating small sensory fibers Aδ, among non-operated non-diabetic obese patients and in the postoperative follow-up (months) M1, 3, 6, 9, 12.
  • Characterization of electromyographic parameters (motor and sensory conduction) in patients with a skin conductance measured by lowered Sudoscan® and / or a threshold of sensitivity to pain increased Thermotest®.
  • Correlation between the presence of a small fiber neuropathy in non-diabetic obese subjects with clinical and biological parameters collected.

Inclusion / non-inclusion:

Inclusion criteria:

morbidly obese patients:

  • BMI 35-55 kg / m²,
  • Male or female,
  • Age> 18 and <60 years,
  • Consultant for the first time at the Centre of obesity of Paris Saint Joseph Hospital Group.

Exclusion criteria:

  • Diabetes known treaty
  • Co-morbidity related to obesity: heart disease, respiratory failure
  • Other causes of peripheral neuropathy:
  • Alcohol Poisoning
  • Renal failure (clearance ≤ 60 mL / min)
  • Infection HIV, hepatitis B, C
  • Deficiencies vitamins B1, B6, B12, folate
  • Treatment with vitamin B6
  • thyroid disease antecedent
  • Previous history of autoimmune disease
  • Previous history of cancer
  • Previous history of neurotoxic treatment (chemotherapy, etc. see list provided in annex)
  • ICU hospitalization antecedent> 48 hours.
  • known history of peripheral neuropathy.

Development of the study:

If patients the eligibility criteria, it will be proposed at the first consultation in central obesity, participate in a clinical study to assess the prevalence of subclinical damage peripheral nerves by simple and painless rapid measurement of skin conductance on the palm of the feet with the Sudoscan® device during the consultation and a Thermotest®, as well as monitoring during the various follow-up consultation after any bariatric surgery or not. This monitoring will be done by the same neurophysiological tests.

  • During the preoperative assessment that will be conducted in the planned hospital in Diabetology Service, written information will be given to patient and no objection will be drawn, then the following tests will be done:
  • The measurement of skin conductance by Sudoscan® and the extent of the painful sensitivity to temperature Thermotest® will be made for all patients included in the study.
  • If the records Sudoscan® skin conductance less than 60μS, we propose a Electroneuromyography the patient as usual on GHPSJ.
  • Measurement of weight, height, waist circumference and hip circumference patient
  • The DN4 scale and Uens clinical neuropathy score.
  • A measurement of blood pressure will be
  • A biological sample will be taken on an empty stomach.
  • For patients with plantar skin conductance will be lowered <60μSiemens and / or whose pain threshold will warm significantly elevated (Thermotest®), if necessary electromyogram will be realized in the second time (appointment given to the output consultation with the endocrinologist.
  • During the postoperative follow-up usually expected for this type of surgery, 1, 3, 6, 9 and 12 months will be made the same clinical examinations than those made during the preoperative assessment and the type of surgery performed. Laboratory tests will be carried out in the usual care for surgical patients.

Methodology Design: prospective, single-center Study duration: 24 months (estimate: 3-5 patients included / week of 15 patients collected in central obesity / week) including 12 months of inclusion.

Number of topics to include: 100 over a period of one year to adjust to the rhythm of the inclusions.

As mentioned, patients will be a measure of impedance of the skin to products chlorine ions by the sweat glands via the Sudoscan®, marketed and used among diabetic patients or not for the detection of violations neuropathic (cf. references and CE certificate attached to the dossier).

The Thermotest® is also marketed and used in diabetic and non-diabetic patients (see references and CE certificate attached to the dossier).

Our center has gained experience of these techniques for the detection of peripheral neuropathy in several patient populations (diabetes and cancer in particular); manipulators (doctors and technicians) are trained in these techniques.

Data collection for each patient:

  • Clinical data:
  • Age
  • Gender
  • BMI
  • Size
  • Weight
  • Waist
  • Hips
  • Report on waist hips
  • Blood pressure: systolic, diastolic, mean
  • Score Questionnaire DN4 (presence or absence of neuropathic pain)
  • Score Uens
  • electrophysiological data
  • skin conductance (μSiemens) measured by the Sudoscan®
  • Plants Average feet (right, left)
  • Thermotest®: average score of sensitivity threshold to pain in plantar warm level (average of the soles of both feet).
  • Electromyography:
  • Sensitive Conduction:
  • sural nerve left and right (lateral malleolus collection, antidromic calf stimulation), radial nerve left and right (wrist collection, antidromic stimulation forearm)
  • Amplitude (mV)
  • VCS (sensory conduction velocity m / s)
  • Motor Conduction:
  • Sciatic nerve popliteal internal right and left (short collection flexor hallucis longus, ankle stimulation)
  • distal motor latency (ms)
  • amplitude of CMAP (mV)
  • Latency wave F shortest (ms).
  • tibial nerve left and right anterior (short collection extensor hallucis longus, ankle stimulation under neck of the fibula, above-neck of the fibula)
  • distal motor latency (ms)
  • Amplitude of PGAM 3 to stimulation points (mV)
  • PNT leg and neck of the fibula (m / s).
  • Latency wave F shortest (ms).
  • EMG needle:
  • Muscles studied: tibialis anterior right, wide left inner, right brachioradialis.
  • Rest Activities: yes / no
  • Activation Pattern:
  • normal Interferential
  • Intermediate with poor temporal summation
  • Poor with temporal summation
  • Single with temporal summation
  • Biological data:
  • Fasting glucose
  • HbA1c
  • Triglycerides
  • Total cholesterol
  • HDL cholesterol
  • LDL Cholesterol
  • uricaemia
  • SGOT, SGPT, gammaGT
  • urea, creatinine
  • creatinine clearance
  • Microalbuminuria on sample
  • serum folate,
  • vitamins D, B1 and B12,
  • calcemia
  • albumin
  • NFS, CRP
  • Electrophoresis + plasma protein immunofixation.

Data processing :

For each subject will be awarded an identifier (original name and surname - year of birth) and the data will be entered on a computer file which will be sent to the statistician in charge of analyzing the GHPSJ site. There will be no exchange of personal data.

Statistical analysis :

The patient will be considered to have a small fiber neuropathy, symptomatic or not, when the skin conductance of chloride ions will be below the threshold for 60μSiemens soles. The prevalence shall be calculated from that definition.

Stratified by age will be made during the statistical analysis.

A test will be performed to analyze the statistical relationship between:

Skin conductance AND

  • BMI,
  • size,
  • Girth
  • Waist circumference ratio / hip circumference
  • Sex,
  • DN4 score,
  • The score Uens,
  • The biological parameters studied: fasting blood glucose, HbA1c, total cholesterol, HDL cholesterol, triglycerides, CRP, serum uric acid.
  • Threshold of pain sensitivity warm on the feet by Thermotest.
  • Type of surgery for surgical patients.

Ethics / Regulatory:

The patient will be informed orally of the objective of the study, a leaflet it will also be provided (attached); its information and not be drawn opposition in his file.

All tests are part of the normal patient care. The ethics of the CPP Ile de France approved this study on march 15th 2015. The manager research center will be the hospital group Paris Saint-Joseph (GHPSJ).

partnerships

Impeto the company, the manufacturer will provide Sudoscan® (loan agreement) the machine for the duration of the study.

GHPSJ ensure the neurologist time, diabetologist, biologist and ARC necessary and will provide the Thermotest® machine for the duration of the study.

Conflicts of interest :

No conflict of interest.

Conditions
Neuropathology
Being tested
Exams
Keywords
Neuropathology

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ExamsDevice

    Patients the eligibility criteria will be proposed at the first consultation in central obesity, participate in a clinical study to assess the prevalence of subclinical damage peripheral nerves by simple and painless rapid measurement of skin conductance on the palm of the feet with the Sudoscan® device during the consultation and a Thermotest®, as well as monitoring during the various follow-up consultation after any bariatric surgery or not. This monitoring will be done by the same neurophysiological tests.

Study groups in NCT02767583
Study groupRoleWhat they receive
Non diabetic obeseExperimentalNon diabetic obese with BMI 35-55 kg / m2 consulting for the first time at the Centre of obesity of Paris Saint Joseph Hospital Group will got a themotest and Sudoscan exams de determine their neuropathology.
Receives: Device: Exams

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Assessment of Chlorine ion production change

    Patients will be a measure of impedance of the skin to products chlorine ions by the sweat glands via the Sudoscan® Device, marketed and used among diabetic patients or not for the detection of violations neuropathic (cf. references and CE certificate attached to the dossier)

    Measured: at inclusion then 1 month, 3 months, 6months and 12 months after surgery

  2. Assessment of Temperature changing sensitivity

    Patients will be measured their sensitivity to temperature changing using the Thermotest Device

    Measured: At inclusion then 1 month, 3 months, 6months and 12 months after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 May 2016 (estimated)
  2. Study start2 Mar 2015
  3. Primary completion30 Jun 2017
  4. Study completion30 Jun 2017

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Screening
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
16 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02767583
Sponsor's protocol ID
Neuropathies and obesity
Acronym
NEUROBISITE
Status last verified
Mar 2018
First submitted
4 May 2016
Last updated
14 Mar 2018
Results posted
No
Data monitoring committee
No

Publications

  • Smith AG, Lessard M, Reyna S, Doudova M, Singleton JR. The diagnostic utility of Sudoscan for distal symmetric peripheral neuropathy. J Diabetes Complications. 2014 Jul-Aug;28(4):511-6. doi: 10.1016/j.jdiacomp.2014.02.013. Epub 2014 Mar 6.

    PubMed 24661818
  • Kopelman PG. Obesity as a medical problem. Nature. 2000 Apr 6;404(6778):635-43. doi: 10.1038/35007508.

    PubMed 10766250
  • Herman RM, Brower JB, Stoddard DG, Casano AR, Targovnik JH, Herman JH, Tearse P. Prevalence of somatic small fiber neuropathy in obesity. Int J Obes (Lond). 2007 Feb;31(2):226-35. doi: 10.1038/sj.ijo.0803418. Epub 2006 Jun 13.

    PubMed 16770330
  • Philippi N, Vinzio S, Collongues N, Vix M, Boehm N, Tranchant C, Echaniz-Laguna A. [Peripheral neuropathies after bariatric surgery]. Rev Neurol (Paris). 2011 Aug-Sep;167(8-9):607-14. doi: 10.1016/j.neurol.2011.01.011. Epub 2011 Apr 22. French.

    PubMed 21514611
  • Thaisetthawatkul P, Collazo-Clavell ML, Sarr MG, Norell JE, Dyck PJ. A controlled study of peripheral neuropathy after bariatric surgery. Neurology. 2004 Oct 26;63(8):1462-70. doi: 10.1212/01.wnl.0000142038.43946.06.

    PubMed 15505166
  • Sumner CJ, Sheth S, Griffin JW, Cornblath DR, Polydefkis M. The spectrum of neuropathy in diabetes and impaired glucose tolerance. Neurology. 2003 Jan 14;60(1):108-11. doi: 10.1212/wnl.60.1.108.

    PubMed 12525727
  • Devigili G, Tugnoli V, Penza P, Camozzi F, Lombardi R, Melli G, Broglio L, Granieri E, Lauria G. The diagnostic criteria for small fibre neuropathy: from symptoms to neuropathology. Brain. 2008 Jul;131(Pt 7):1912-25. doi: 10.1093/brain/awn093. Epub 2008 Jun 4.

    PubMed 18524793
  • Casellini CM, Parson HK, Richardson MS, Nevoret ML, Vinik AI. Sudoscan, a noninvasive tool for detecting diabetic small fiber neuropathy and autonomic dysfunction. Diabetes Technol Ther. 2013 Nov;15(11):948-53. doi: 10.1089/dia.2013.0129. Epub 2013 Jul 27.

    PubMed 23889506

Questions about this trial

What is this clinical trial studying?

A study testing Exams in people with Neuropathology, run by Fondation Hôpital Saint-Joseph at 1 site in France.

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 5 inclusion and 14 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: finished, as of the sponsor's last update on 14 Mar 2018. 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 France. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Assessment of Chlorine ion production change (time frame: at inclusion then 1 month, 3 months, 6months and 12 months after surgery). The study lists 2 primary outcomes in all. 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 NCT02767583, which also lists 8 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 14 Mar 2018.

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