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Intermittent Claudication clinical trials

View clinical trials related to Intermittent Claudication.

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NCT ID: NCT00914316 Completed - Clinical trials for Peripheral Arterial Disease

Supervised Treadmill Exercise And Ranolazine For Intermittent Claudication Of Lower Extremities

STERILE
Start date: May 2009
Phase: N/A
Study type: Interventional

The goal of this study is to evaluate whether supervised treadmill exercise combined with ranolazine 1000 mg twice daily provides an incremental benefit in absolute walking distance over supervised exercise alone in patients with stable claudication. Investigators also seek to determine if the administration of ranolazine provides a sustained benefit after the completion of a supervised exercise regimen. Lastly, investigators wish to determine whether both exercise and ranolazine improves peak oxygen consumption and anaerobic threshold in patients with stable claudication.

NCT ID: NCT00906022 Completed - Clinical trials for Severe Intermittent Claudication

Self Expanding Nitinol Stent Versus Percutaneous Transluminal Arterial Angioplasty (PTA) With Optional Bailout Stenting in Case of PTA Failure in Patients With Symptomatic Critical Limb Ischemia or Severe Intermittent Claudication (EXPAND)

EXPAND
Start date: May 2009
Phase: Phase 4
Study type: Interventional

The clinical investigation is a prospective, international, multi-centre, randomized (1:1) trial with follow up investigations at 1, 3, 6 and 12 months. Patients will be randomized either to treatment with stenting with the Astron Pulsar SE (4 or 5 mm diameter) stent or to PTA with optional bailout stenting in case of PTA failure. The primary objective of this study is to show clinical improvement in the outcome of patients with symptomatic critical limb ischemia or severe intermittent claudication (Rutherford 3, 4, 5) treated with the Astron Pulsar SE (4 or 5 mm diameter) in comparison with PTA or optional bailout stenting in case of PTA failure.

NCT ID: NCT00905359 Completed - Spinal Stenosis Clinical Trials

Neurogenic Intermittent Claudication Evaluation Study

NICE
Start date: January 2010
Phase: Phase 4
Study type: Interventional

The objective of the NICE study is to provide clinical evidence proving that the Aperius™ PercLID™ System is safe and non-inferior to standalone decompressive surgery with regards to clinical outcomes in patients suffering from Degenerative Lumbar Spinal Stenosis with Neurogenic Intermittent Claudication, relieved by flexion.

NCT ID: NCT00895635 Completed - Clinical trials for Intermittent Claudication

Evaluating Two Exercise Training Programs to Reduce Leg Pain in People With Peripheral Arterial Disease (The EXERT Study)

EXERT
Start date: January 2009
Phase: Phase 3
Study type: Interventional

Peripheral arterial disease (PAD) is a disorder that affects more than 8 million people in the United States. As a result of decreased blood flow to the legs, people with PAD may experience leg pain and difficulty with walking. This study will examine the effectiveness of two exercise programs—a treadmill walking program and an aerobic arm exercise program—at increasing walking distance and decreasing leg pain in people with PAD.

NCT ID: NCT00887744 Completed - Spinal Stenosis Clinical Trials

Intermittent Neurogenic Claudication Treatment With APERIUS®

INCA
Start date: November 2006
Phase: Phase 4
Study type: Interventional

The primary purpose of the study is to measure the change in severity of symptoms and ability to function in every day activities in patients suffering from degenerative lumbar spinal stenosis after treatment with the Aperius® device.

NCT ID: NCT00883246 Completed - Clinical trials for Peripheral Arterial Disease

Study of SilverHawk®/TurboHawk® in Lower Extremity Vessels (DEFINITIVE™ LE)

Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the intermediate and long-term effectiveness of stand-alone atherectomy treatment of peripheral arterial disease in the legs.

NCT ID: NCT00879697 Completed - Hypertension Clinical Trials

Strength Training in Walking Tolerance in Intermittent Claudication Patients

Start date: July 2005
Phase: Phase 3
Study type: Interventional

Background: Muscle atrophy and reduced leg strength are related to exercise intolerance in patients with intermittent claudication (IC), suggesting that strength training (ST) could improve exercise performance in these patients. Objective: Analyze the effects of ST in walking capacity in patients with IC comparing with walking training (WT) effects. Intervention: Patients were randomized into ST and WT. Both groups trained twice a week, for 12 weeks, at the same rate of perceived exertion. ST consisted of 3 sets of 10 repetitions of whole body exercises. WT consisted of 15 two-minute bouts of walking intercalated with 2 minutes of resting. Measurements: Walking capacity, peak VO2, walking economy, ankle brachial index, ischemic window and knee extension strength

NCT ID: NCT00834548 Completed - Atherosclerosis Clinical Trials

Whole-Body MRA at 3T - A Comparison Between Two Different Scan Protocols

Start date: June 2008
Phase: N/A
Study type: Observational

To compare to different approaches in whole-body magnetic resonance angiography of patients suffering peripheral arterial disease. Our hypothesis is that use of a new protocol improves the diagnostic quality of the WB-MRA procedure.

NCT ID: NCT00822172 Completed - Clinical trials for Peripheral Arterial Disease

Evaluation of Cilostazol in Combination With L-Carnitine

ECLECTIC
Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see how safe and effective L carnitine taken with cilostazol is compared to placebo taken with cilostazol for people with intermittent claudication. A second purpose of the study is to see if L-carnitine is absorbed into the blood stream.

NCT ID: NCT00798850 Completed - Clinical trials for Intermittent Claudication

Trial of Nonsurgical Treatment of Intermittent Claudication Due to Femoro-popliteal Disease

Start date: August 2002
Phase: N/A
Study type: Interventional

Intermittent Claudication (IC)is a common condition characterised by pain in the muscles of the legs on exertion caused by "hardening of the arteries" and a reduced blood supply. The investigators know that the vast majority of people suffering from this condition remain stable and do not deteriorate, and thus in general the viability of legs is not at risk. The main aim of treatment, therefore, is to try and improve walking thus reducing the impact this problem has on patients life style. There are many methods of management of intermittent claudication, but the investigators do not know which produces the best results. This study aims to compare the short and medium term outcomes of exercise programmes, percutaneous transluminal angioplasty and a combination of the two treatments for patients with intermittent claudication.