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Intermittent Claudication Clinical Trials

A listing of Intermittent Claudication medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (25) clinical trials

PREFERred Exercise Modalities in Patients With Intermittent Claudication

Supervised exercise programme consisting of 2 hours per week for 12 weeks are recommended as first-line treatment for intermittent claudication. However, the programmes are not always available and when they are the uptake and adherence is poor, with time being cited as the greatest barrier to participation. One benefit of ...

Phase N/A

Arm-crank Exercise Training on Cardiovascular Function of Patients With Peripheral Artery Disease

12 weeks of ACE training on cardiovascular function in PAD patients, and compare it with treadmill exercise (TE), the actual recommendation for this patients. In this clinical trial, 4 patients will be allocated randomly in three experimental groups: ACE training, TE and control group. ACE and TE groups will perform ...

Phase N/A

Assessing the Feasibility of Including Patients With Peripheral Artery Disease in to an Established Cardiac Rehabilitation Service.

Peripheral artery disease (PAD) is a progressive disease that occurs as the result of atherosclerotic plaque formation in the major arteries of the leg (Mays, Casserly and Regesteiner, 2013). The main presenting symptom of PAD is intermittent claudication (IC) - exertional pain or discomfort in the calf, thigh or buttock ...

Phase N/A

Pain Management and Patient Education for Physical Activity in Intermittent Claudication (PrEPAID)

Peripheral Arterial disease (PAD) affects 2.7 million people in the United Kingdom (UK). The most common symptom that patients experience is Intermittent Claudication (IC), which is pain in the buttock, calf or thigh precipitated by exercise and relieved by rest. The underlying cause of PAD is atherosclerosis, which leads to ...

Phase N/A

Distributed Registry

The purpose of this study is to test if a patient can be directly connected to a quality assurance (QA) database, traditionally known as a registry. Patient-reported outcomes (PRO) data will be entered into the database directly from a patient's mobile phone from their index procedure for 12 months. The ...

Phase N/A