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Chronic Venous Insufficiency clinical trials

View clinical trials related to Chronic Venous Insufficiency.

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NCT ID: NCT03283800 Completed - Varicose Veins Clinical Trials

Copper Impact on Venous Insufficiency and Lipodermatosclerosis

CIVIL
Start date: September 23, 2015
Phase: N/A
Study type: Interventional

Venous disease has an adverse impact on the quality of life of patients and the NHS spends considerable resources on this chronic condition. Copper has been shown to promote new blood vessel formation and therefore improve blood supply to the affected area and possibly skin conditions. Copper has also been shown to have strong antimicrobial properties. We plan to perform a study whereby patients who would normally be given leg stockings will be asked to wear similar stockings except that one of the stockings will contain copper fibers. Neither the patient nor the clinician will know which is which. Photographs of the leg conditions will be taken at baseline, 2, 4 and 8 weeks to evaluate healing. Benefit will be evaluated by a symptom questionnaire, severity scoring tools and healing scores taken from the serial photographs.

NCT ID: NCT03104985 Completed - Clinical trials for Chronic Venous Insufficiency

LLLT of Trophic Ulcers of Lower Extremities and Chronic Venous Insufficiency

Start date: May 2013
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate comparatively the efficiency of traditional treatment methods in patients with chronic venous diseases of C6 class, and a new combined low level laser therapy (LLLT) by LASMIK device. The results of outpatient examination and treatment of patients with venous trophic ulcers, observed in the City Polyclinic of "Tula Municipal Clinical Hospital №2" were analyzed.

NCT ID: NCT02395302 Completed - Venous Leg Ulcer Clinical Trials

Evaluation of a Dual Action Pneumatic Compression System: Tolerance and Comfort in Patients With Venous Leg Ulcers

Start date: December 2014
Phase: N/A
Study type: Interventional

The purpose of the study is to assess treatment tolerance and comfort in chronic VLUs after 4 weeks of treatment using a dual action pneumatic compression device.

NCT ID: NCT02346058 Completed - Clinical trials for Chronic Venous Insufficiency

Efficacy and Safety of Esarin Gel in Chronic Venous Insufficiency and Varicose Veins

Start date: October 2013
Phase: Phase 4
Study type: Interventional

Evaluation efficacy and safety of Esarin Gel in subjects with chronic venous insufficiency or varicose veins combine superficial vein thrombophlebitis.

NCT ID: NCT02236338 Completed - Clinical trials for Chronic Venous Insufficiency

Radiofrequency Ablation vs Laser Ablation of the Incompetent Greater Saphenous Vein

Start date: September 2008
Phase: Phase 4
Study type: Interventional

The aim of this study is to perform a randomized, prospective trial comparing the two current methods of treatment for chronic venous insufficiency, in an effort to evaluate complications and outcomes for each method, and ultimately, to see if one is superior to the other.

NCT ID: NCT02215369 Completed - Clinical trials for Chronic Venous Insufficiency

SeCure Endovenous Laser Treatment Study

SeCure
Start date: January 2015
Phase: N/A
Study type: Interventional

The VenaCure EVLT 400 µm Fiber Kit is currently marketed for the treatment of varicose veins. AngioDynamics, Inc., the company that manufacturers the VenaCure device, is sponsoring this study to assess the safety and effectiveness of the VenaCure EndoVenous Laser Treatment (EVLT) 400 µm Fiber Kit for treatment of incompetent perforator veins (IPVs). The VenaCure EVLT 400 µm Fiber Kit has not been previously studied by AngioDynamics for the ablation of IPVs.

NCT ID: NCT02050061 Completed - Clinical trials for Chronic Venous Insufficiency

Chronic Venous Insufficiency; Impact of Compression Stockings on Quality of Life

Start date: November 2011
Phase: N/A
Study type: Interventional

Chronic venous insufficiency (CVI) is a common disease affecting mainly lower limbs leading to significant impact on the quality of life. There is no study, to our knowledge, has attempted to evaluate the impact of compression stockings on all patients with CVI. Our aim is to estimate the prevalence of CVI in Qassim Region and to test the effectiveness of compression stockings.

NCT ID: NCT02015221 Completed - Clinical trials for Chronic Venous Insufficiency

Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort

Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the ease of use and comfort of the ACTitouch dual action pneumatic compression device in patients with unilateral or bilateral chronic venous insufficiency (CVI) with or without venous leg ulcers, as compared to standard compression.

NCT ID: NCT01899482 Completed - Clinical trials for Chronic Venous Insufficiency

Manual Lymphatic Drainage in Chronic Venous Insufficiency: a Randomized Controlled Trial

MLDCVI
Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare functional status and quality of life of a group of patients with chronic venous insufficiency treated with manual lymphatic drainage with a group not treated with manual lymphatic drainage. Investigators hypothesized that manual lymphatic drainage can improve: - quality of life, - functional status, - calf muscle strength, - ankle range of motion, - edema, - severity of disease, - and symptoms.

NCT ID: NCT01848210 Completed - Clinical trials for Chronic Venous Insufficiency

Efficacy and Safety of Coumarin and Troxerutin in the Symptomatic Treatment of Chronic Venous Insufficiency

Start date: May 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of the fixed-dose combination of coumarin and troxerutin versus placebo in the symptomatic treatment of chronic venous insufficiency.