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Venous Insufficiency clinical trials

View clinical trials related to Venous Insufficiency.

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NCT ID: NCT05504070 Enrolling by invitation - Clinical trials for Chronic Venous Insufficiency

Venclose digiRF System Post Market Study

Start date: September 8, 2023
Phase: N/A
Study type: Interventional

A Post-Market, Multi-Center, Prospective, Interventional Study for Treatment of Chronic Venous Disease of the Great and Small Saphenous Veins and Incompetent Perforator Veins.

NCT ID: NCT05449743 Recruiting - Clinical trials for Chronic Venous Insufficiency

Assessment of the Effect of Spa Therapy on the Quality of Life of Patients With Chronic Venous Insufficiency (NEYRAC)

NEYRAC
Start date: July 11, 2022
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of a phlebology-oriented spa therapy at 6 months on the quality of life of patients suffering from chronic venous insufficiency of the lower limbs

NCT ID: NCT05383469 Completed - Clinical trials for Chronic Venous Insufficiency

Efficacy of Active Versus Passive Methods in Chronic Venous Insufficiency

Start date: September 13, 2022
Phase: N/A
Study type: Interventional

The aim of our study was to compare the effectiveness of active and passive practices in patients with CVI.

NCT ID: NCT05364112 Recruiting - Varicose Ulcer Clinical Trials

Utilization of Compreflex Wraps in Patients With Chronic Venous Insuffciency

Start date: September 1, 2021
Phase: N/A
Study type: Interventional

This is a multicentre, quasi-experimental study to evaluate the Conformitè Europëenne-marked Compreflex standard calf and foot (with basic liner) under routine conditions. The study will be conducted at 4 clinics and will include 100 consecutive patients. Patients will be followed-up until 26 weeks.

NCT ID: NCT05058989 Completed - Varicose Veins Clinical Trials

The Evaluation of the Pathophysiology of Varicose Veins in Pregnancy

Start date: June 1, 2021
Phase:
Study type: Observational

Varicose veins (VV) are the early sign of Chronic venous insufficiency (CVI) which are characterised by abnormal tortuosity and dilatation of superficial veins of lower limb extremities. Factors for the development of VV exist in literature. However, the exact mechanism remains unclear. The prevalence of VV are greater in women compared to men and also higher in pregnant women compared to non-pregnant women which make pregnant women at higher risk of developing VV. Furthermore, complications of VV have negative impacts on patients' quality of life and health care budget. Therefore, better understanding of the cause of VV can contribute in better quality of life to the patient and provide valuable insights to help in reducing health care cost. The present study will investigate the contribution of both mechanical and chemical factors in pregnant women by taking blood samples for genomic testing, using Duplex ultrasound, vector flow imaging, limb volume assessment using Truncated cone tool, assessment of iliac vein compression using Photoplethysmography (PPG) technique, hormonal blood test and assessing patient's quality of life using Aberdeen Varicose Veins Questionnaire (AVVQ).

NCT ID: NCT05051540 Recruiting - Clinical trials for Chronic Venous Insufficiency

The Effect of Inelastic Compression System on Quality of Life in People With Chronic Venous Insufficiency

Start date: November 15, 2021
Phase: N/A
Study type: Interventional

The purpose of this protocol is to measure the effect of the use of an inelastic compression system (ICS) on quality of life (QOL) in patients with chronic venous insufficiency (CVI) who have demonstrated limited or no compliance with prescribed compression stockings or bandage wraps.

NCT ID: NCT05047302 Withdrawn - Clinical trials for Chronic Venous Insufficiency

Investigation of Femoropopliteal In Situ Valve Formation With the InterVene System-Canada

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

Prospective, non-randomized, multicenter pre-market feasibility study to evaluate subjects treated with the BlueLeaf System for the treatment of symptomatic CVI of the lower extremity.

NCT ID: NCT05005052 Recruiting - Clinical trials for Chronic Venous Disease

Sulodexide in the Treatment of Chronic Primary Venous Disease of the Lower Extremities

SuloPrima
Start date: November 25, 2021
Phase: Phase 3
Study type: Interventional

This study compares the efficacy and safety of sulodexide (Vessel) to placebo in patients with chronic venous disease of the lower extremities. The primary hypothesis is that more patients will achieve a decrease in rVCSS score of at least 4 points with sulodexide than with placebo.

NCT ID: NCT04995432 Recruiting - Venous Leg Ulcer Clinical Trials

Non Contrast MRI in Lower Extremity

Start date: January 1, 2018
Phase:
Study type: Observational

We collected retrospectively the non contrast MRI in chia yi memorial hospital for different venous disease of lower extremity morphology and flow ananlysis were done.

NCT ID: NCT04943172 Recruiting - Clinical trials for Deep Venous Insufficiency (Diagnosis)

The Hancock Jaffe Surgical Antireflux Venous Valve Endoprosthesis Study

Start date: August 27, 2021
Phase: N/A
Study type: Interventional

A prospective, non blinded, single arm, multicenter study designed to assess the safety and effectiveness of the bioprosthetic, VenoValve, which is surgically implanted into the deep venous system for treatment of patients with deep venous valvular insufficiency ( C4b-C6 patients).