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Peripheral Vascular Diseases clinical trials

View clinical trials related to Peripheral Vascular Diseases.

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NCT ID: NCT03615833 Completed - Clinical trials for Peripheral Arterial Disease

Pilot Study of Vitamin D Screening Use in Peripheral Arterial Disease Patient Over Maximum Distance Walking

First-BLINDOS
Start date: March 11, 2019
Phase: Phase 4
Study type: Interventional

The prevalence of peripheral arterial disease (PAD) is greater than 15%. PAD is associated with an increased risk of cardiovascular death, coronary heart disease and stroke, with a mortality rate of 5% per year. Most clinical evidence supports the idea that having normal vitamin D reduces cardiovascular risk. The data suggests that normalizing vitamin D levels would have a significant impact on public health, reduce costs and help control the incidence and prevalence of cardiovascular disease. There is also a plausible physiological theory, supported by numerous observational studies, that vitamin D supplementation should be effective in improving cardiovascular outcomes, such as blood pressure, arterial stiffness, atherosclerosis, endothelial function, and clinical events. The investigators hypothesize that routine screening for vitamin D deficiency and supplementation in case of hypovitaminosis D is effective for improving the maximum walking distance after 12 weeks of treatment in stage 2 PAD patients .

NCT ID: NCT03606629 Completed - Clinical trials for Peripheral Arterial Disease

SOLARIS Endoprosthesis in Iliac Occlusive Disease

SOLARIS I
Start date: March 1, 2019
Phase:
Study type: Observational

Fifty patients will be treated with Solaris Endoprosthesis and followed up to 2 years with Walking Impairment Questionnaire and Doppler Ultrasound evaluation in 30 days, 6 months and 12 months.

NCT ID: NCT03590769 Completed - Clinical trials for Peripheral Arterial Disease

Arterial Imaging of Inflammation and Resolution After Endovascular Surgery

AIIRES
Start date: June 1, 2017
Phase: Phase 1
Study type: Interventional

This study evaluates the local inflammatory and resolution response of patients undergoing peripheral vascular intervention like an angioplasty of the superficial femoral artery (SFA) or popliteal artery, or stenting of the iliac artery or SFA, through the use of Positron emission tomography-magnetic resonance imaging (PET/MRI). PET/MRI will be performed prior to intervention, one day and one week after intervention.

NCT ID: NCT03585387 Completed - Clinical trials for Peripheral Arterial Disease

Cardiac Positioning System in Peripheral Angioplasty Procedure.

MDG-Periph
Start date: February 27, 2019
Phase:
Study type: Observational

This clinical investigation is intended to evaluate the ability of a magnetic cardiac positioning system to decrease medical radiation exposure on a peripheral angioplasty procedure in patients with a peripheral artery stenosis.

NCT ID: NCT03570788 Completed - Quality of Life Clinical Trials

HRQoL Among Patients Amputated Due to Peripheral Arterial Disease

Start date: September 12, 2014
Phase:
Study type: Observational

A prospective cohort study over the prosthetic use among patients amputated after vascular disease and the impact of their HRQoL.

NCT ID: NCT03564080 Completed - Clinical trials for Coronary Artery Disease

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

Start date: July 18, 2018
Phase: N/A
Study type: Interventional

This study will investigate if patients with peripheral artery disease (PAD) can be successfully incorporated into an already existing Cardiac Rehabilitation programme. One group of PAD patients will exercise as a group, and the other group will exercise alongside patients with coronary artery disease (CAD).

NCT ID: NCT03511612 Completed - Clinical trials for Peripheral Arterial Disease, Ankle Brachial Index, Doppler

Comparison of the Ankle-Brachial Index Measurement Using a Specific Oscillometric Device vs. the Doppler Method

ABIOSCILLO
Start date: April 24, 2018
Phase: N/A
Study type: Interventional

Several methods are available to measure ankle brachial index (ABI) non-invasively. A recent scientific statement of the AHA considers the Doppler method as the reference. However because Doppler devices are not widely available in primary care, several attempts have been made to propose alternative methods, among whom oscillometric methods (automatic blood pressure machines) have attracted most attention. We hypothesize that: - the diagnostic characteristics (i.e. sensitivity, specificity and AUC) of the oscillometric method would be very good as compared to the Doppler method. the oscillometric method would have better intra- and inter-observer reproducibilities as compared to the Doppler method.

NCT ID: NCT03511157 Completed - Clinical trials for Peripheral Arterial Disease

Ischemic Preconditioning Claudication Study

Start date: June 14, 2018
Phase: N/A
Study type: Interventional

This study proposes ischemic preconditioning (IPC) as a novel intervention to improve walking distance in patients with intermittent claudication.

NCT ID: NCT03510676 Completed - Clinical trials for Peripheral Arterial Disease

The ILLUMINA Study. (ILLUMINA)

ILLUMINA
Start date: January 26, 2016
Phase: N/A
Study type: Interventional

The aim of the prospective, multicentre, single-arm study is to assess safety and efficacy of a drug eluting stent in Nitinol alloy (NiTiDES) in term of vessel patency and composite event-free survival rate up to two years follow-up in focal/medium length lesions in patients with ischemic obstruction of superficial femoral arteries or/and proximal popliteal arteries.

NCT ID: NCT03496948 Completed - Clinical trials for Cardiovascular Diseases

Telephone Health Coaching and Remote Exercise Monitoring for Peripheral Artery Disease

TeGeCoach
Start date: April 23, 2018
Phase: N/A
Study type: Interventional

Peripheral artery disease (PAD) is the third most prevalent cardiovascular disease worldwide, with over 200 million people affected. Most prominent symptom is leg pain while walking known as intermittent claudication. Based on the currently existing gaps in the management of intermittent claudication, the objective of the this study is to explore the clinical effectiveness and cost advantage of TeGeCoach, a 12-month long home-based exercise program, compared to usual care. TeGeCoach consists of telephone health coaching, remote walking exercise monitoring based on wearable activity monitors and intensified primary care. It is hypothesized that TeGeCoach will improve functional outcomes and will reduce total health care costs.