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Intermittent Claudication clinical trials

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NCT ID: NCT00403494 Completed - Clinical trials for Intermittent Claudication

A Phase 2 Study of the Effects of Sapropterin Dihydrochloride on Symptomatic Peripheral Arterial Disease

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate whether sapropterin dihydrochloride is safe and effective in the treatment of intermittent claudication (IC) caused by peripheral arterial disease (PAD).

NCT ID: NCT00399919 Completed - Clinical trials for Intermittent Claudication

Safety and Efficacy of Propionyl-L-Carnitine in the Treatment of Peripheral Arterial Disease (Intermittent Claudication)

Start date: April 2006
Phase: Phase 3
Study type: Interventional

Patients with peripheral artery disease have decreased blood flow to exercising muscle causing pain. This decreased blood flow to the muscle affects the level of acylcarnitines which in turn decreases the level of carnitine. Carnitine allows muscles to function properly. This study will test the safety and efficacy of Propionyl-L-Carnitine taken in combination with a monitored exercise training program.

NCT ID: NCT00388128 Completed - Clinical trials for Intermittent Claudication

Caffeine and Intermittent Claudication

Start date: September 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the change in Walking capacity after an intake of caffeine. The study design is cross-over and follow-up of 80 patients with leg pain caused by narrowing of their leg arteries, Peripheral Vascular Disease (PAD), stage II. Half of all will be revascularised, follow up will be after 3 months. It is hypothesized that caffeine (6mg/kg) can be a cheap, safe drug before walking exercise. Primary endpoint is maximum walking distance (MWD), treadmill-testing,(constant load, 0%,2m/h). Secondary endpoints are pain free walking distance (PWD), maximum muscle strength, endurance, reaction speed, balance, cognitive function, health related quality of life (SF-36).

NCT ID: NCT00352222 Completed - Thrombosis Clinical Trials

Safety and Efficacy of Express LD to Treat Stenosed or Occlusive Atherosclerotic Disease in Iliac Arteries

MELODIE
Start date: January 2004
Phase: Phase 3
Study type: Interventional

To obtain additional data on safety and efficacy of the Express stent implantation in the treatment of stenosed or occlusive atherosclerotic disease (de novo or restenotic lesions) in the iliac arteries (common or external).

NCT ID: NCT00351286 Active, not recruiting - Clinical trials for Peripheral Arterial Disease

Efficacy Study of Oral L-Citrulline in Patients Taking Simvastatin With Peripheral Arterial Disease

Start date: March 2006
Phase: Phase 2
Study type: Interventional

To prove the combination of L-citrulline with simvastatin leads to greater improvement in the symptoms of peripheral arterial disease (PAD) than simvastatin alone by evaluating oral L- citrulline or placebo against simvastatin for improvement in treadmill walking distance in patients, 40–75 years of age, who have PAD with intermittent claudication.

NCT ID: NCT00311805 Active, not recruiting - Clinical trials for Peripheral Artery Disease

Autologous CD34+ Stem Cell Injection for Severe Intermittent Claudication (Leg Pain)

Start date: April 2006
Phase: Phase 1
Study type: Interventional

The goal of the study is to determine the safety and possible effectiveness of various doses of autologous (one's own) stem cells, delivered with a needle into the regions of the leg with poor blood flow in patients with blocked leg arteries that results in claudication (pain when walking). Stem cells are primitive cells produced by the bone marrow that can develop into blood cells or other types of cells. In addition to determining whether this new approach is safe, the diagnostic tests may offer preliminary insights into the usefulness of this approach for treating intermittent claudication - the condition where areas in the leg are lacking enough oxygen and blood flow to keep the leg muscle working well, causing pain and cramping upon walking. This study is a double-blind, randomized study to compare CD34-positive stem cells versus a placebo agent (salt water solution known as normal saline). The patient will have a 3:1 chance of their stem cells versus the placebo. Regardless of a patient receiving placebo or treatment, all patients will undergo all of the pre-treatment phases of this study, which includes the stem cell mobilization and apheresis procedure.

NCT ID: NCT00300690 Completed - Clinical trials for Critical Limb Ischemia

Choice of Material for Above-Knee Femoro-Popliteal Bypass Prosthetic Graft (PopUp)

Start date: October 1993
Phase: Phase 4
Study type: Interventional

This trial was designed to challenge the wide held view that polytetrafluoroethylene (PTFE) performs better than Dacron for above knee femoropopliteal bypass.

NCT ID: NCT00300339 Completed - Clinical trials for Intermittent Claudication

Mixed Antagonist of Serotonin for Claudication Optimal Therapy

MASCOT
Start date: February 2006
Phase: Phase 2
Study type: Interventional

To investigate in patients suffering from intermittent claudication due to Fontaine stage II PAD whether a 24-week treatment by SL650472 OD on top of clopidogrel may result in an improvement of walking capacity, by comparing three doses of SL650472 to placebo, and to calibrate such effect versus cilostazol

NCT ID: NCT00279994 Active, not recruiting - Clinical trials for Intermittent Claudication

(Cost) Effectiveness Study of Exercise Therapy in Patients With Peripheral Arterial Disease

EXITPAD
Start date: December 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if supervised exercise therapy in a physiotherapeutic setting, with or without therapy feedback, is more (cost-)effective than exercise therapy based on a 'go home and walk' advice without supervision, for patients with PAD stage II (Fontaine).

NCT ID: NCT00274157 Terminated - Clinical trials for Peripheral Vascular Disease

FIRE-PAD: Functional Improvement Through Revascularization of the Extremities for Peripheral Arterial Disease

Start date: March 2007
Phase: Phase 2
Study type: Observational

The specific aims of the project are as follows: To determine whether catheter-based revascularization procedures improve functional capacity and quality of life among patients with intermittent claudication. To investigate whether improvements in walking ability result in a less sedentary lifestyle and improvement of the cardiovascular risk profile.