Type 2 DiabetesPhase 4NCT00902616
Effect of Arginine on Microcirculation in Patients With Diabetes
A Phase 4 study testing L-arginine in people with Type 2 Diabetes, run by Tameside Hospital NHS Foundation Trust at 1 site in United Kingdom.
Trial summary
Patients with diabetes have dysfunction of the lining of the arteries which lead to impaired circulation in the small blood vessels. This is thought to be secondary to reduced chemicals in the blood viz: nitric oxide. This chemical is derived from an amino acid (protein) L-arginine. Read more about this study
- Who is it for?
- Ages 30 to 65 years
- Conditions the study is for
- Type 2 Diabetes
- What is being tested?
- L-arginine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 40 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- Jun 2003to Jun 2006
- Phase
- Phase 4
- 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 30 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Males and females diabetic patients with peripheral neuropathy, aged 30-65 years
- Type 2 diabetes (NIDDM) judged by WHO criteria:
- onset of diabetes mellitus after the age of 30 years
- not requiring insulin for control of diabetes or insulin treatment initiated after one year diagnosis of diabetes
- no history of diabetic ketoacidosis
- All patients will have detailed history and physical examination
Who cannot join
- Patients with ischaemic heart disease
- Previous stroke and severe peripheral vascular disease)
- Previous amputation
- Renal failure (defined as serum creatinine > 120 mmol/l)
- Uncontrolled hypertension (BP > 160/90)
- Patients on nitrates
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site
Tameside General Hospital
Ashton-under-Lyne, Cheshire, OL6 9RW
About this study
Official title: L-Arginine and Endothelial Dysfunction in Type 2 Diabetic Patients
Patients with diabetes have dysfunction of the lining of the arteries which lead to impaired circulation in the small blood vessels. This is thought to be secondary to reduced chemicals in the blood viz: nitric oxide. This chemical is derived from an amino acid (protein) L-arginine. Therefore, the researchers investigated whether giving patients L-arginine (versus dummy powder) would improve the blood flow in the small blood vessels in the lower limbs of patients with damage to their nerves (neuropathy).
Read the detailed description
Peripheral neuropathy is one of the most common complications of diabetes mellitus (DM) with a prevalence of around 30 - 45%. In addition, diabetic patients are at increased risk of macrovascular disease, as well as other complications such as retinopathy and nephropathy.
The majority of patients will have developed peripheral neuropathy 10-20 years after the onset of diabetes, which is an important cause of foot ulceration, Charcot joints, amputation and increased morbidity and mortality. In view of this the cost to the National Health Service in 1987 was a staggering £13.5 million. Therefore there is an urgent need for prevention of diabetic neuropathy and its sequelae.
The exact pathogenesis of diabetic neuropathy is unclear, with both metabolic and vascular factors having been implicated. Microvascular disease is possibly the initial event in the development of diabetic complications. Microvascular disease may play an important role in the causation and exacerbation of diabetic neuropathy. Histopathological studies have shown thickening of vessel walls, hyperplasia of capillary endothelial cells and increased plugging of vessels in neuropathic patients. Endothelial dysfunction is thought to be an important initiating factor for the development of these complications. Endothelial dysfunction is thought to develop as a consequence of changes in nitric oxide and cell adhesion molecules in the plasma of diabetic patients. L-arginine is an amino acid, which is the only source of NO in the body.
We therefore propose to study the efficacy of arginine supplementation ( this is available over the counter as a food supplement) on endothelial function and other biomarkers of impaired endothelial function. We hope with this study to demonstrate that L-arginine supplementation will enhance nitric oxide availability, thereby improve the microcirculation and subsequently improve peripheral nerve function. We will use surrogate markers to assess the efficacy of L-arginine supplementation to show an improvement in diabetic complications such as microalbuminuria in the urine, and TcPO2 in the skin of the lower limbs. In addition microcirculation will be assessed using the Moor Laser Doppler flow machine and the Radiometer TcPO2 device. Endothelial function will also be assessed indirectly by measuring the cell adhesion molecules ICAM-1, VCAM-1, P-selectin and E-selectin. This will be performed using standard ELISA techniques.
A total of 40 patients will be recruited for the study. Half will be randomised to taking the food supplement L-arginine and half to placebo. At baseline all patient will have a clinical assessment of their neuropathy status in the lower limb, blood pressure and BMI. Fasting bloods for glucose, lipids profile, U\&E's, FBC, CRP, cell adhesion molecules and nitric oxide will be done at baseline and three months later at the end of the study. The TcPO2 and micro-circulation will be assessed at baseline and also at three month.
Each of the twenty patients that is randomised to L-arginine will be given a tin containing 1 kilogram of the food supplement L-arginine. They are to take a spoonful (three grams) of the L-arginine and dissolve it in a glass of sugar free cold drink of their choice such as orange or lemon squash. They are to take it before food three times a day. The twenty patient randomised to placebo will receive a tin containing one kilogram of placebo and the instruction is as for the L-arginine group.
20 patients will receive L-arginine powder (3G TDS) and 20 patients will receive placebo, lactose powder (3G TDS)
Clinical examination as part of routine care:
- BMI, BMI will be calculated by weight/height (kg/m2).
- Lying and standing blood pressure will be measured twice, in the right arm using Dinamap™ (Critikon, UK), after resting for 10 minutes. Hypertension will be defined according to WHO criteria (systolic blood pressure (sBP) >140 mm Hg and/or diastolic blood pressure (dBP) >90 mm Hg or if the patient is on current antihypertensive treatment.
- Overnight microalbumin excretion rate.
- Neuropathic Disability Score and Vibration Perception threshold.
Additional examination:
- TcPO2 of the right foot.
- Micro-circulation of the right foot using Moore Laser Doppler iontophoresis.
Blood from an antecubital vein will be collected after an overnight fast and after resting for fifteen minutes in the supine position for:
- as part of routine care - FBC, U\&E's, fasting glucose, glycated haemoglobin, fasting lipid profile
- additional blood test - CRP, cell adhesion molecules, nitric oxide
- Conditions
- Type 2 Diabetes
- Being tested
- L-arginine, Placebo Lactose powder
- Keywords
- Type 2 diabetes, Peripheral neuropathy, Microcirculation
- Medical subject headings
- Diabetes Mellitus, Type 2, Peripheral Nervous System Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
L-arginineDietary supplement
3gm TDS for three months
Placebo Lactose powderDietary supplement
3gm TDS for 3 months
| Study group | Role | What they receive |
|---|---|---|
| 1. L-arginine | Active comparator | 3 gm TDS for 3 months Receives: Dietary Supplement: L-arginine |
| 2. Placebo - Lactose powder | Placebo comparator | 3 gm TDS for 3 months Receives: Dietary Supplement: Placebo Lactose powder |
What is being measured
The primary outcome is the main question the study is designed to answer.
Improvement in microcirculation
Measured: 3 months
Secondary outcomes (1)
Effect of L-arginine on clinical parameters of neuropathy
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 May 2009 (estimated)
- Study startJun 2003
- Primary completionJun 2006
- Study completionJun 2006
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Type 2 DiabetesStudies 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
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 40 participants (actual)
Sponsor and investigators
- Lead sponsor
- Tameside Hospital NHS Foundation Trust
- Sponsor type
- University, hospital or other
- Investigators
- Edward Jude, MD, MRCP, Principal investigator, Tameside General Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00902616
- Sponsor's protocol ID
- Arginine01
- Status last verified
- May 2009
- First submitted
- 12 May 2009
- Last updated
- 27 Nov 2013
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 27 Nov 2013. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- L-Arginine and Endothelial Dysfunction in Type 2 Diabetic Patients
- ClinicalTrials.gov ID
- NCT00902616
- Acronym / sponsor ID
- Arginine01
- Conditions
- Type 2 Diabetes
- Keywords
- Type 2 diabetes, Peripheral neuropathy, Microcirculation
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 40 participants (actual)
- Lead sponsor
- Tameside Hospital NHS Foundation TrustUniversity, hospital or other
- Study start
- Jun 2003
- Primary completion
- Jun 2006 (actual)
- Study completion
- Jun 2006 (actual)
- First posted
- 15 May 2009 (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.
Patients with diabetes have dysfunction of the lining of the arteries which lead to impaired circulation in the small blood vessels. This is thought to be secondary to reduced chemicals in the blood viz: nitric oxide. This chemical is derived from an amino acid (protein) L-arginine. Therefore, the researchers investigated whether giving patients L-arginine (versus dummy powder) would improve the blood flow in the small blood vessels in the lower limbs of patients with damage to their nerves (neuropathy).
Detailed description
Peripheral neuropathy is one of the most common complications of diabetes mellitus (DM) with a prevalence of around 30 - 45%. In addition, diabetic patients are at increased risk of macrovascular disease, as well as other complications such as retinopathy and nephropathy.
The majority of patients will have developed peripheral neuropathy 10-20 years after the onset of diabetes, which is an important cause of foot ulceration, Charcot joints, amputation and increased morbidity and mortality. In view of this the cost to the National Health Service in 1987 was a staggering £13.5 million. Therefore there is an urgent need for prevention of diabetic neuropathy and its sequelae.
The exact pathogenesis of diabetic neuropathy is unclear, with both metabolic and vascular factors having been implicated. Microvascular disease is possibly the initial event in the development of diabetic complications. Microvascular disease may play an important role in the causation and exacerbation of diabetic neuropathy. Histopathological studies have shown thickening of vessel walls, hyperplasia of capillary endothelial cells and increased plugging of vessels in neuropathic patients. Endothelial dysfunction is thought to be an important initiating factor for the development of these complications. Endothelial dysfunction is thought to develop as a consequence of changes in nitric oxide and cell adhesion molecules in the plasma of diabetic patients. L-arginine is an amino acid, which is the only source of NO in the body.
We therefore propose to study the efficacy of arginine supplementation ( this is available over the counter as a food supplement) on endothelial function and other biomarkers of impaired endothelial function. We hope with this study to demonstrate that L-arginine supplementation will enhance nitric oxide availability, thereby improve the microcirculation and subsequently improve peripheral nerve function. We will use surrogate markers to assess the efficacy of L-arginine supplementation to show an improvement in diabetic complications such as microalbuminuria in the urine, and TcPO2 in the skin of the lower limbs. In addition microcirculation will be assessed using the Moor Laser Doppler flow machine and the Radiometer TcPO2 device. Endothelial function will also be assessed indirectly by measuring the cell adhesion molecules ICAM-1, VCAM-1, P-selectin and E-selectin. This will be performed using standard ELISA techniques.
A total of 40 patients will be recruited for the study. Half will be randomised to taking the food supplement L-arginine and half to placebo. At baseline all patient will have a clinical assessment of their neuropathy status in the lower limb, blood pressure and BMI. Fasting bloods for glucose, lipids profile, U\&E's, FBC, CRP, cell adhesion molecules and nitric oxide will be done at baseline and three months later at the end of the study. The TcPO2 and micro-circulation will be assessed at baseline and also at three month.
Each of the twenty patients that is randomised to L-arginine will be given a tin containing 1 kilogram of the food supplement L-arginine. They are to take a spoonful (three grams) of the L-arginine and dissolve it in a glass of sugar free cold drink of their choice such as orange or lemon squash. They are to take it before food three times a day. The twenty patient randomised to placebo will receive a tin containing one kilogram of placebo and the instruction is as for the L-arginine group.
20 patients will receive L-arginine powder (3G TDS) and 20 patients will receive placebo, lactose powder (3G TDS)
Clinical examination as part of routine care:
- BMI, BMI will be calculated by weight/height (kg/m2).
- Lying and standing blood pressure will be measured twice, in the right arm using Dinamap™ (Critikon, UK), after resting for 10 minutes. Hypertension will be defined according to WHO criteria (systolic blood pressure (sBP) >140 mm Hg and/or diastolic blood pressure (dBP) >90 mm Hg or if the patient is on current antihypertensive treatment.
- Overnight microalbumin excretion rate.
- Neuropathic Disability Score and Vibration Perception threshold.
Additional examination:
- TcPO2 of the right foot.
- Micro-circulation of the right foot using Moore Laser Doppler iontophoresis.
Blood from an antecubital vein will be collected after an overnight fast and after resting for fifteen minutes in the supine position for:
- as part of routine care - FBC, U\&E's, fasting glucose, glycated haemoglobin, fasting lipid profile
- additional blood test - CRP, cell adhesion molecules, nitric oxide
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 1. L-arginine | Active comparator | Dietary Supplement: L-arginine3 gm TDS for 3 months |
| 2. Placebo - Lactose powder | Placebo comparator | Dietary Supplement: Placebo Lactose powder3 gm TDS for 3 months |
Who may qualify
- Ages
- 30 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Males and females diabetic patients with peripheral neuropathy, aged 30-65 years
- Type 2 diabetes (NIDDM) judged by WHO criteria:
- All patients will have detailed history and physical examination
Key exclusion criteria (6 listed)
- Patients with ischaemic heart disease
- Previous stroke and severe peripheral vascular disease)
- Previous amputation
- Renal failure (defined as serum creatinine > 120 mmol/l)
- Uncontrolled hypertension (BP > 160/90)
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 |
|---|---|---|
| L-arginine3gm TDS for three months | Dietary supplement | 1. L-arginine |
| Placebo Lactose powder3gm TDS for 3 months | Dietary supplement | 2. Placebo - Lactose powder |
Primary outcome
Improvement in microcirculation
Time frame: 3 months
1 secondary outcome
Effect of L-arginine on clinical parameters of neuropathy
Time frame: 3 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Nov 2013.
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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.
Edward Jude, MD, MRCP principal investigator
Tameside General Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing L-arginine in people with Type 2 Diabetes, run by Tameside Hospital NHS Foundation Trust 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 6 inclusion and 6 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 27 Nov 2013. 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Improvement in microcirculation (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 27 Nov 2013.