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Chronic Venous Insufficiency clinical trials

View clinical trials related to Chronic Venous Insufficiency.

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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: NCT02248740 Terminated - Clinical trials for Chronic Venous Insufficiency

Radiofrequency Ablation vs. Laser Ablation of the Incompetent Small 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 related to the Small Saphenous Vein (SSV) to evaluate complications and outcomes for each method, and ultimately, to see if one is superior to the other.

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.

NCT ID: NCT01654016 Completed - Clinical trials for Chronic Venous Insufficiency

Study of Antiinflammatory Effects of Detralex (Daflon)

Start date: August 2012
Phase: Phase 4
Study type: Interventional

Aim of the study: To investigate if there is a differences in expression of inflammatory markers in venous wall and blood among patients treated with Detralex and those not treated with Detralex (control group).

NCT ID: NCT01574911 Recruiting - Lymphedema Clinical Trials

Validation of a New Method of Limb Volumetry

Start date: April 2012
Phase: N/A
Study type: Observational

Volumetry is essential for the diagnosis and follow-up of patients with limb edema. The objective of this project is the validation of real-time reconstruction and calculation of limb volume using a 3D laser scanner. Water - displacement volumetry (water-filled boot) is the reference method with known accuracy and reproducibility, but is not commonly used in clinical practice because it is cumbersome, difficult, and time-consuming. The most commonly used method remains segmental limb perimetry with a tape measure, followed by volume calculation using the truncated cones formula, thus excluding de facts extremities (hands and feet) which can neither be likened to cones nor easily measured. Quantification limb volume and volume changes is essential for the diagnosis and follow-up of patients with chronic venous insufficiency or lymphedema, two very common pathological conditions. It is mandatory for the evaluation of therapeutic approaches. The present study will use an innovative technology of volume acquisition by freehand laser scanning with a hand-held camera with Quantification limb volume and volume changes is essential for the diagnosis and follow-up of patients with chronic venous insufficiency or lymphedema, two very common pathological conditions. It is mandatory for the evaluation of therapeutic approaches. The present study will use an innovative technology of volume acquisition by freehand laser scanning with a hand-held camera with real-time 3D reconstruction. Its advantages are non-contact, accurate and detailed quantification of edema, including extremities, allowing to assess the magnitude and topography of physiological, pathological, or treatment - induced volume changes. This approach will ultimately provide data that will used for designing personalized limb compression ortheses.