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Varicose Veins clinical trials

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NCT ID: NCT02593799 Completed - Liver Cirrhosis Clinical Trials

Non-invasive Prediction of Esophageal Varices in Liver Cirrhosis: A Multicenter Observational Study

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

Esophageal variceal bleeding is one of the most lethal complications of liver cirrhosis. In the early stage of liver cirrhosis, the prediction of esophageal varices is very important for guiding the clinical decision making of primary prophylaxis of variceal bleeding.

NCT ID: NCT02584842 Completed - Bleeding Clinical Trials

Rivaroxaban in Endovenous Laser Ablation With and Without Miniphlebectomy

RITE
Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of this study is to determine retrospectively if the application of rivaroxaban after endovenous laser ablation with and without miniphlebectomy is safe and if it lowers the risk of venous thrombosis.

NCT ID: NCT02558426 Completed - Varicose Veins Clinical Trials

Estrogen Receptors and Chronic Venous Disease

ERCVD
Start date: January 2015
Phase: N/A
Study type: Observational

Chronic Venous Disease (CVD) is a very common problem affecting western adult population. To date the pathophysiology of CVD development encloses several theories such as the role of extracellular matrix (ECM) components alterations, the alteration of Matrix Metalloproteinases (MMPs) and other related molecules, the endothelial dysfunction, and several genetic factors but none of these could properly explain its genesis. Estrogen Receptors may be involved in CDV pathogenesis. Endogenous estrogens are important regulators of vascular homeostasis and they act mainly via three different ERs which are expressed in the cardiovascular system: ERα, ERβ, and a G protein-coupled estrogen receptor termed GPER. of this study is to explore the expression of estrogen receptors in vessel wall of varicose veins through the entire clinical spectrum of CVD.

NCT ID: NCT02522845 Completed - Varicose Veins Clinical Trials

Compression Therapy Following Endothermal Ablation

COMETA
Start date: May 2015
Phase: N/A
Study type: Interventional

This study will be looking at the effect of compression therapy in patients having endovenous treatment for truncal incompetence of their varicose veins using either radiofrequency ablation (RFA) or endovenous laser therapy (EVLT). 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: NCT02504684 Completed - Varicose Veins Clinical Trials

Treatment of Saphenous Vein Reflux With 1920-nm Diode Laser

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

Objective: Compare venous occlusion rates at a one-year follow-up comparing 1920-nm versus 1470-nm laser treatment. Design: Non-randomized prospective study. Methods: Adult patients with varicose veins associated with great saphenous reflux were included. Procedures were performed between February and April of 2013. The 1470-nm laser ablation was performed in continuous mode, power being set between 8 and 10 W, while for the 1920-nm it was set between 5 and 6 W. Checking for vein closure was performed during the thermal ablation procedure, LEED (linear endovenous energy density) being calculated after the procedure. Follow-up data were collected at the 7-day, 30-day, 3-month, 6-month and 1-year visits, and involved clinical and ultrasound evaluation, measurement of occlusion extent.

NCT ID: NCT02465645 Completed - Clinical trials for Cirrhosis With Esophageal Varices

To Compare the Efficacy and Safety of Carvedilol With or Without Simvastatin in Patients With Portal Hypertension and Esophageal Varices.

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

After successful screening of patients based on inclusion criteria, we will measure the baseline Hepatic Venous Pressure Gradient. At day 1 patients will undergo complete blood investigation including complete haemogram, kidney function test, liver function test, prothrombin time, AFP (Alfa Feto Protein) level, chest x ray, ultrasonography, fibroscan. Routine complete physical examination will be done.

NCT ID: NCT02462720 Completed - Varicose Veins Clinical Trials

COMFORT: A Multicenter, Open-label, Randomized, Crossover Study

COMFORT
Start date: May 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate pain the patient experienced following treatment of varicose veins with Varithena® compared to radiofrequency ablation.

NCT ID: NCT02454452 Completed - Varicose Veins Clinical Trials

Comparison of Radiofrequency, Vein Stripping and CHIVA for Venous Insufficency

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

Randomized controlled clinical trial aimed to compare the effectiveness and safety of radiofrequency, saphenous vein stripping and conservative hemodynamic treatment of venous insufficiency (CHIVA) in the treatment of saphenous varicose veins, in terms of absence of saphenous vein reflux, patient quality of life and post-surgical complications.

NCT ID: NCT02441881 Completed - Varicose Veins Clinical Trials

Trial of Radiofrequency Thermo-ablation Treatments of Great Saphenous Varicose Veins (3-RF Study)

Start date: September 5, 2014
Phase: N/A
Study type: Interventional

A double blind randomised controlled trial of radiofrequency thermal ablation treatments of great saphenous varicose veins: Venefit (Closurefast), vs. Radiofrequency induced Thermal Therapy vs. Endovenous Radiofrequency. Assessments by visual pain scores, duplex ablation and quality of life questionaires

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.