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Chronic Venous Insufficiency clinical trials

View clinical trials related to Chronic Venous Insufficiency.

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NCT ID: NCT04236245 Completed - Clinical trials for Chronic Venous Insufficiency

EU Post Market Clinical Follow-Up Study of the Venclose System for Saphenous Vein Incompetence

Start date: May 11, 2020
Phase: N/A
Study type: Interventional

This is a prospective, non-randomized study in which patients who meet eligibility criteria and consent to participate will undergo a minimally invasive procedure using radiofrequency (RF) energy for ablation of the great saphenous vein (GSV).

NCT ID: NCT04231942 Recruiting - Varicose Veins Clinical Trials

Elastic Compression Stockings and Varicose Veins Recurrence

ECOS-VVR
Start date: December 16, 2019
Phase: N/A
Study type: Interventional

Hypothesis. Regular using of Class 1 below-knee graduated compression stockings (RAL GZ 387 standard) compared to the absence of elastic compression will reduce the risk of clinically significant varicose veins recurrence at 12 months after endovenous thermal ablation of the great saphenous vein and elimination of varicose tributaries.

NCT ID: NCT04054440 Enrolling by invitation - Clinical trials for Peripheral Arterial Disease

Outpatient Office Based Endovascular Procedures

Start date: June 20, 2014
Phase:
Study type: Observational

The results of this study will serve as a starting point for future trials concentrating on the effectiveness and clinical outcomes of the procedures performed in an office based angiosuite. Additionally, other studies could compare clinical outcomes between procedures performed in an office based angiosuite and other settings.

NCT ID: NCT03904602 Terminated - Clinical trials for Chronic Venous Insufficiency

EdemaWear to Reduce Edema in Hospitalized Patients With CVI:

Start date: August 19, 2019
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to evaluate the effectiveness of EdemaWear® fuzzy wale longitudinal compression stockings on reducing lower extremity edema in hospitalized adult patients with a history of CVI who are at high risk of consequent venous leg ulcers (VLU) and patient experience with continuously wearing Edema Wear for up to five days

NCT ID: NCT03900234 Completed - Clinical trials for Chronic Venous Insufficiency

Prevalence of Chronic Venous Disease in General Population

Start date: July 1, 2015
Phase:
Study type: Observational

This study is designed to find prevalence and risk factors for chronic venous disease (CVD) in the general population. All the resident, who live in a single rural settlement will be invited to participate.

NCT ID: NCT03893201 Completed - Varicose Veins Clinical Trials

A Singapore Venaseal Real World Post-Market Evaluation Study

ASVS
Start date: April 11, 2018
Phase:
Study type: Observational

The study aims to assess the efficacy of VenaSealâ„¢ Closure System (VCS) for the treatment of lower extremity superficial truncal veins in a real-world clinical setting, in a multi-racial Asian population in Singapore.

NCT ID: NCT03835559 Recruiting - Clinical trials for Chronic Venous Insufficiency

Cyanoacrylate Closure Versus Surgical Stripping for Incompetent Saphenous Veins

CASS
Start date: April 10, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the non-inferior, clinical outcomes after cyanoacrylate closure comparing the surgical stripping for incompetent saphenous veins.

NCT ID: NCT03784131 Recruiting - Clinical trials for Chronic Venous Insufficiency

Tissue Engineered Veins in Patients With Chronic Venous Insufficiency

TECVI-1
Start date: December 15, 2021
Phase: Phase 1
Study type: Interventional

This study aims to evaluate the safety (incidence of adverse events including serious adverse events and clinical significant laboratory abnormalities) of personalized tissue engineered veins (P-TEV) with valves implanted in patients with severe chronic venous insufficiency (CVI). For each patient a segment of the femoral vein containing the non-functioning valve will be surgically replaced with a single P-TEV containing a functioning valve.

NCT ID: NCT03685838 Recruiting - Varicose Veins Clinical Trials

Compression Stockings Therapy Following Mechano-Chemical Ablation (Clarivein®)

COMMOCA
Start date: February 13, 2019
Phase: N/A
Study type: Interventional

This study will be looking at the effect of compression therapy in patients having Mechano-Chemical Ablation (MOCA) therapy for truncal incompetence of their varicose veins using the ClariVein® device. Patients will be randomised to either the compression group (group A) or the no compression group (group B). The pain scores, compliance, quality of life scores, occlusion rate at 6 months as well as the cost effectiveness of each intervention will be assessed.

NCT ID: NCT03562546 Recruiting - Clinical trials for Chronic Venous Insufficiency

The Effect of Structured Exercise on Chronic Venous Insufficiency

CVI
Start date: August 1, 2018
Phase: N/A
Study type: Interventional

Individuals with Chronic Venous Insufficiency (CVI) face a number of complications, such as, muscular dysfunction, limited ankle range of motion(ROM) and diminished calf muscle pump function. Exercise therapy has been shown to improve calf muscle pump function and symptoms and may provide additional therapeutic benefits. It has been reported that structured exercise has the ability to improve ankle joint range of motion, calf muscle strength and calf muscle pump function. Participants will receive the 12-week structured resistance exercise programme, 'Strength from Within', a warm up and cool down, walking programme and range of motion exercises. Participants will complete the Short Form quality of life (SF-36) Health Survey and the venous clinical severity score questionnaire. Baseline testing will be conducted. The following measures will be employed in the study through a baseline testing and repeated at the end of the study period (week 12): Functional ambulatory measurements, physical activity measurements (muscle endurance), isokinetic testing (strength), duplex ultrasound scanning. A combination of upper and lower body structured exercise as well as, ankle join range of motion and a walking regimen has the potential to have a significant impact on an individual's calf muscle pump function and avoid these potentially harmful side effects of lower body exercise programmes