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Varicose Veins clinical trials

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NCT ID: NCT01332838 Unknown status - Varicose Veins Clinical Trials

A Comparison of Specialized Versus Standard Compression After Saphenous Ablation

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

The purpose of this study is to determine if the use of specialized compression garments, in comparison to standard compression, improves early patient outcomes after endovenous ablation.

NCT ID: NCT01287702 Recruiting - Varices Clinical Trials

Early Feeding Following Ligation of Acute Bleeding Varices

Start date: January 2011
Phase: Phase 4
Study type: Interventional

The impact of feeding after endoscopic treatment of gastroesophageal varices has never been investigated. It is still unknown whether early feeding may increase early rebleeding in patients with acute esophageal variceal bleeding treated with EVL. It is customary for clinicians to institute fasting for 2 or 3 days after emergency EVL. This may be a safe approach to watch against early rebleeding. However, many patients would be fasting for a longer time and nutrition may be impaired, possibly resulting in aggravation of ascites. Thus, the investigators conduct a controlled study to evaluate whether early feeding have a bad impact on patients receiving emergency EVL or histoacryl injection for bleeding gastric varices.

NCT ID: NCT01231373 Completed - Varicose Veins Clinical Trials

Polidocanol Endovenous Microfoam (PEM) Versus Vehicle for the Treatment of Saphenofemoral Junction (SFJ) Incompetence

VANISH-2
Start date: November 2010
Phase: Phase 3
Study type: Interventional

Varicose veins are enlarged, noticeably bulging veins, which commonly occur in the legs and may cause discomfort. In this study, patients with varicose veins in the legs will be participating. The purpose of this research study is to evaluate the safety and effectiveness of three different concentrations of an investigational drug, Polidocanol Endovenous Microfoam (PEM) compared to vehicle (inactive solution) in treating the symptoms and appearance of varicose veins.

NCT ID: NCT01203397 Withdrawn - VARICOSE VEINS Clinical Trials

Safety And Efficacy Study Of Topic Mucopolysaccharide Polysulfate In The Superficial Varicose Veins Treatment

Start date: September 2014
Phase: Phase 3
Study type: Interventional

Evaluate the safety, tolerability and effectiveness of mucopolysaccharide polysulfate in the treatment of superficial varicose veins

NCT ID: NCT01200199 Completed - Varicose Veins Clinical Trials

Validity of Electronic Diary for Monitoring Varicose Veins Symptoms

Start date: November 2010
Phase:
Study type: Observational

The purpose of this study is to contribute to the validation of an electronic daily diary to assess symptoms in patients with varicose veins.

NCT ID: NCT01197833 Completed - Clinical trials for Great Saphenous Vein Incompetence

Endovenous Ablation With and Without Polidocanol Endovenous Microfoam Treatment for Patients With Great Saphenous Vein Incompetence and Visible Varicosities

017
Start date: September 2010
Phase: Phase 3
Study type: Interventional

Varicose veins are enlarged, noticeably bulging veins, which commonly occur in the legs and may cause discomfort. In this study, patients with varicose veins in the legs will be participating. The purpose of this research study is to evaluate the safety and effectiveness of two different doses of an investigational drug, Polidocanol Endovenous Microfoam (PEM) compared to vehicle (inactive solution) when used following an approved heat treatment in subjects with varicose veins.

NCT ID: NCT01195623 Completed - Varicose Veins Clinical Trials

The Long-term Value of Preoperative Duplex Before Surgery for Varicose Veins

Start date: November 1997
Phase: N/A
Study type: Interventional

Duplex imaging is costly and time-consuming, but is used increasingly for preoperative evaluation of varicose veins. Its value in terms of the long-term results of surgery is not clear. 293 patients (343 limbs) with primary varicose veins were randomized to operation with or without preoperative duplex imaging. Reoperation rates, clinical and duplex findings were compared at 2 months and 2 years after surgery. Routine preoperative duplex examination led to an improvement in results. However two years is a short time, and with a longer follow-up other mechanisms for recurrence may become more important, e.g. neovascularization (new vessel formation) or progression of disease, hence the value of a detailed preoperative diagnosis may be diminished. The aim of this phase of the investigation is to study the results after 8 years, in particular what mechanisms for recurrences were most important.

NCT ID: NCT01173419 Withdrawn - Varicose Veins Clinical Trials

Comparison Study for Safety and Efficacy of Two Devices for the Treatment of the Great Saphenous Vein

RECoN
Start date: July 2010
Phase: N/A
Study type: Interventional

This is a multi center, randomized, comparison study using two already cleared methods of treatment of the great saphenous vein (GSV). The hypothesis to be tested is that the use of the Venacure EVLT NeverTouch procedure is no worse than the RF ClosureFAST procedure for treatment of the GSV. Evaluation of post operative pain and bruising, quality of life assessments, adverse event assessments, confirmation of long term GSV closure, use of medications are criteria that will be evaluated during the course of this study.

NCT ID: NCT01103258 Completed - Clinical trials for Varicose Vein Disease

FOAM-study, Cost Minimization Study Comparing Surgery Versus Duplex Guided Foam Sclerotherapy of Varicose Veins

Start date: February 2006
Phase: N/A
Study type: Interventional

Varicose vein disease is a common health problem, which causes much discomfort to patients. Nowadays treatment modalities for greater saphenous veins include surgery and duplex guided foam sclerotherapy. These are two equally accepted and applied treatments for the same patient population. Choice of treatment often depends on the referral preference of the General Practitioner. Until now data are missing which treatment is more cost effective. The current proposal aims at comparing the effects, costs and patient preferences between duplex guided foam sclerotherapy and surgery in the treatment of greater varicose veins.

NCT ID: NCT01072877 Completed - Varicose Veins Clinical Trials

Efficacy and Safety Study of Polidocanol Injectable Foam for the Treatment of Saphenofemoral Junction (SFJ) Incompetence

VANISH-1
Start date: December 2010
Phase: Phase 3
Study type: Interventional

Varicose veins are enlarged, noticeably bulging veins, which commonly occur in the legs and may cause discomfort. In this study, patients with varicose veins in the legs will be participating. The purpose of this research study is to evaluate the safety and effectiveness of three different concentrations of an investigational drug, polidocanol injectable foam compared to vehicle (inactive solution) in treating the symptoms and appearance of varicose veins.