L-Citrulline in Peripheral Artery Disease

NCT ID: NCT02521220

Last Updated: 2019-09-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 49 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-08-01
• Study Completion Date: 2019-08-30

Brief Summary

Some studies have reported improved vascular function with the supplementation of L-arginine in participants with cardiovascular disease (CVD). Several clinical studies have also begun the investigation of L-arginine supplementation in participants with peripheral artery disease (PAD). This is particularly important as currently there are limited options available to medically manage intermittent leg pain resulted from PAD. Although some of these short-term clinical trials suggested that oral L-arginine improved walking distance or improved walking speed in participants with PAD, these results were not consistent. Further, only 1% of the oral supplemented L-arginine is available for the NO production as the rest is metabolised by the body. A better way to provide the body with substrate to produce NO is therefore needed. The natural amino acid and food component, L-citrulline has been suggested to be a good candidate for this purpose.

L-citrulline, named after watermelon citrullus vulgaris from which it was first isolated, is a natural precursor of L-arginine. Studies have shown that L-citrulline is metabolised by the body to a lesser degree compared to L-arginine and hence is an effective precursor of arginine in peripheral tissues, including endothelial cells. Oral L-citrulline supplementation also eliminates some of the unwanted effects associated with oral arginine supplementation and it is well tolerated without known side effects. In addition, L-citrulline is a supplement that is available over-the-counter. Thus, oral supplementation of L-citrulline may be a new intervention strategy in participants with PAD.

The investigators hypothesize that the oral food supplement L-citrulline, unlike L-arginine, reverses endothelial dysfunction. In a multinational, multicenter, double blinded, randomised, placebo-controlled cross-over trial the effects of L-citrulline in peripheral artery disease will be investigated.

Detailed Description

The primary aim of this trial is to examine whether the oral food supplement L-citrulline has any effect on clinical status, walking distance, arterial and endothelial function in participants with PAD.

The investigators will use a double-blinded crossover design in which patients serve as their own controls. Patients who are enrolled will have two 'treatment' periods of twelve weeks with a wash-out period of 4 weeks in between. Patients will be randomly assigned to get L-citrulline in the first and placebo in the second period and vice versa.

After a screening phase of 3 weeks, there will be a 'zero-point' measurement en then the first 'treatment' period of 12 weeks starts (placebo or food-supplement). Then there is a wash-out phase of 4 weeks after which the second 'treatment' period starts (food-supplement or placebo) In both periods, after 2 weeks and at the end of the period, a measurement of primary and secondary outcomes will be done: a questionnaire has to be filled out, treadmill test and flow-mediated dilation (for vessel function). The follow-up will take another 4 weeks and will end with a phone call to check for the condition of the patient and possible side effects.

Since every patient gets both placebo and the food-supplement, every patient is his/her own control.

The study was completed with 24 patients in Hannover, Germany, and 25 in Melbourne, Australia.

Conditions

Peripheral Arterial Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

L-citrulline

Oral food-supplemental amino-acid L-citrulline. 2 times 3g per day.

Group Type: EXPERIMENTAL

L-citrulline

Intervention Type: DIETARY_SUPPLEMENT

L-citrulline 2 times daily 3 gram (6g/day)

Maltodextrin

Maltodextrin as placebo. 2 times 3g per day

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DIETARY_SUPPLEMENT

Maltodextrin 2 times daily 3 gram (6g/day)

Interventions

L-citrulline

L-citrulline 2 times daily 3 gram (6g/day)

Intervention Type: DIETARY_SUPPLEMENT

Placebo

Maltodextrin 2 times daily 3 gram (6g/day)

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• 40 years or older males and postmenopausal women;
• male participants must agree to using an adequate form of contraception during the study period;
• 6-month history of stable intermittent claudication (IC) due to PAD;
• PAD secondary to atherosclerosis with significant claudication (Fontaine class II defined as IC, or Fontaine class III defined as pain at rest);
• IC characterised by pain, ache, cramp, numbness or severe fatigue involving muscles of one or both lower extremities, reproducibly provoked by walking and relieved by rest;
• ankle-brachial index (ABI) at rest of <0.9 and at least 25% decrease in ABI within 1 min during exercise recovery;
• capacity to walk more than 2 min/15 meters but no more than 12 min on a treadmill using the Skinner-Gardner protocol;
• walking limited by claudication, not coexisting conditions; and
• difference between two consecutive baseline exercise treadmill tests of <25% during the 3-weeks run-in period; and
• no change in medications or physical activity within 3 months prior to enrolment.

Exclusion Criteria

• Women of child-bearing potential;
• Current enrolment in another clinical trial and/or ingestion of another investigational product within the past 30 days before enrolment;
• PAD of non-atherosclerotic nature;
• Fontaine class IV i.e. ulcer or gangrene;
• leg amputation above the ankle;
• peripheral vascular surgery, sympathectomy, peripheral angioplasty or stent insertion within the previous 3 months;
• myocardial infarction, unstable angina, percutaneous transluminal coronary angioplasty or coronary artery bypass graft surgery within the previous 3 months;
• uncontrolled hypertension (resting systolic blood pressure (SBP) >190 or diastolic blood pressure (DBP) >115 mmHg);
• hypotension (SBP <90mmHg);
• type I diabetes, proliferative retinopathy;
• history of disease state or surgery that affects gastrointestinal absorption;
• significant renal disease (serum creatinine >3.0 mg/dl);
• liver disease (transaminase > 3x upper limit of normal, bilirubin >1.5 times upper limits of normal);
• history of treatment for any malignancy within the past 5 years, or evidence of active malignancy other than squamous cells or basal cell carcinoma of the skin;
• serious infection or hypotension associated with sepsis in the last month;
• cerebrovascular infarct in the last 3 months;
• autoimmune disorders (e.g. systemic lupus erythematosis, ulcerative colitis);
• any other acute or chronic medical condition that in the opinion of the investigators increases the likelihood that the participant would be unable to complete the study;
• unwillingness to discontinue arginine- or L-citrulline-containing products, pentoxifylline, L-carnitine, or prostacyclin for at least 1 month prior to and during the study; and
• conditions other than PAD that limit walking distance.

• Minimum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Clinical Trial Center Maastricht B.V.

OTHER

Sponsor Role: collaborator

Catharina Ziekenhuis Eindhoven

OTHER

Sponsor Role: collaborator

Hannover Medical School

OTHER

Sponsor Role: collaborator

Maastricht University

OTHER

Sponsor Role: lead

Responsible Party

H. Schmidt

Prof.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Harald Schmidt, Prof.

Role: PRINCIPAL_INVESTIGATOR

Maastricht University

Locations

Hannover Medical School

Hanover, , Germany

Maastricht University

Maastricht, Limburg, Netherlands

Catharina Ziekenhuis Eindhoven

Eindhoven, , Netherlands

Countries

Germany; Netherlands

Other Identifiers

CIPER2015UM

Identifier Type: -

Identifier Source: org_study_id