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Peripheral Vascular Diseases clinical trials

View clinical trials related to Peripheral Vascular Diseases.

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NCT ID: NCT00827619 Completed - Clinical trials for Peripheral Arterial Disease (PAD)

Zilver® Flex™ Vascular Stent Study

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

This study is intended to evaluate the long-term effectiveness of treatment of de novo or restenotic lesions of the above-the-knee femoropopliteal artery using the Zilver® Flex™ Vascular Stent which has received the CE mark for commercial use. The study is designed as a single arm non-randomized post-approval study.

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: NCT00821028 Completed - Atherosclerosis Clinical Trials

Local Paclitaxel Delivery for SFA Disease

IRRITAX
Start date: January 2009
Phase: N/A
Study type: Interventional

To see if restenosis rates of superficial femoral artery atherosclerosis with percutaneous techniques can be improved using paclitaxel.

NCT ID: NCT00819598 Completed - Clinical trials for Peripheral Arterial Disease

Pilot Study to Determine the Optimal Technique for Measurement of Ankle Blood Pressures

Start date: January 2009
Phase: N/A
Study type: Observational

Peripheral arterial disease (PAD) is a highly prevalent medical condition. Patients with PAD are usually diagnosed on the basis of the ankle-brachial index. The ankle-brachial index is the ratio of ankle pressure to arm pressure based on measurement of blood pressures in the arms and legs using a Doppler device. The need for dedicated equipment and trained personnel, along with the time required to perform the test, have been identified as barriers to widespread implementation of ankle-brachial index screening. The use of automated oscillometric devices for blood pressure measurement and determination of the ankle-brachial index has been applied with variable success. It will be beneficial to investigate a reliable oscillometric-based procedure that can accurately measure leg pressures for the ankle-brachial index across the entire spectrum of PAD severity. The purpose of this study is to determine the optimal oscillometric-based technique for estimation of Doppler-derived systolic arm and ankle blood pressures for calculation of the ankle-brachial index in patients with and without PAD. Subjects with suspected arterial disease in the non-invasive lab will be enrolled. Arm, ankle, and toe pressure measurements will be made in the supine position using Doppler, oscillometric methods, and photoplethysmographic sensor. Arm and ankle pressures from a subset of subjects will be obtained in both seated and supine positions. The ankle-brachial index and toe-brachial index will be calculated.

NCT ID: NCT00817349 Completed - Clinical trials for Coronary Artery Disease

Angio-Seal Evolution Device Registry

Start date: July 2008
Phase:
Study type: Observational

Collect data on the use of the Angio-Seal Evolution Device in diagnostic and interventional patient populations.

NCT ID: NCT00814970 Completed - Clinical trials for Peripheral Vascular Disease

The Complete® SE SFA Study for the Treatment of SFA/PPA Lesions

Start date: November 2008
Phase: N/A
Study type: Interventional

To evaluate the safety and efficacy of the Complete SE SFA Stent System in the treatment of de novo and/or restenotic lesions or occlusions in the Superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) in subjects with symptomatic Peripheral Artery Disease (PAD).

NCT ID: NCT00809497 Completed - Clinical trials for Peripheral Arterial Disease

A Clinical Study on Efficacy & Safety Profile of Propionyl-L-carnitine Tablets for Peripheral Arterial Diseases

PLC
Start date: May 2008
Phase: Phase 3
Study type: Interventional

The main objective of this study is to evaluate the effectiveness and safety of the propionyl-L-carnitine hydrochloride tablets among Chinese population in comparison with the placebo, for treatment of the peripheral arterial diseases (intermittent claudication) with oral supplementation of 2g daily for a 4 months continuous administration.

NCT ID: NCT00797056 Completed - Clinical trials for Peripheral Vascular Diseases

Stem Cell Mobilization by G-CSF to Treat Severe Peripheral Artery Disease

STEMPAD
Start date: April 2008
Phase: Phase 0
Study type: Interventional

This study is designed to test the use of G-CSF in peripheral vascular disease. The investigators hypothesize that mobilization of angiogenic cells into the blood by granulocyte colony stimulating factor (G-CSF) may stimulate the formation of new blood vessels and result in a sustained improvement in blood flow in patients with severe peripheral arterial disease.

NCT ID: NCT00781950 Active, not recruiting - Clinical trials for Peripheral Arterial Disease

Effects of Dietary Flaxseed on Symptoms of Cardiovascular Disease in Patients With Peripheral Arterial Disease

FLAXPAD
Start date: October 2008
Phase: Phase 2/Phase 3
Study type: Interventional

This Clinical Trial is being conducted to study how patients with peripheral arterial disease (a condition in which the blood vessels of the extremities are affected) respond to a dietary regimen of flaxseed. The purpose of the study is to examine whether or not dietary flaxseed have any effect on improving symptoms of cardiovascular disease. Additionally, the effects of dietary flaxseed on exercise tolerance will be assessed.

NCT ID: NCT00778336 Completed - Thrombosis Clinical Trials

A Prospective Observational Registry of Peripheral Use of AngioJet Rheolytic Thrombectomy With Mid-Length Catheters

Start date: January 2007
Phase: N/A
Study type: Observational

This registry collects observational data about how mid-length AngioJet catheters (ie XPEEDIOR and DVX models) are used in routine clinical practice.