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Varicose Veins clinical trials

View clinical trials related to Varicose Veins.

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NCT ID: NCT01942941 Completed - Varicose Veins Clinical Trials

Peripheral Vascular Disease and Nerve Stimulation

CCLINS
Start date: June 2013
Phase: N/A
Study type: Interventional

A study to see what effect the geko™ device has on blood flow in patients with lower limb vascular disease.

NCT ID: NCT01936168 Completed - Clinical trials for Greater Saphenous Vein Injury

MOCA Versus RFA in the Treatment of Primary Great Saphenous Varicose Veins

MARADONA
Start date: December 1, 2016
Phase: N/A
Study type: Interventional

The newly developed Mechanochemical Endovenous Ablation (MOCA) device uses a technique that combines mechanical endothelial damage using a rotating wire with the infusion of a liquid sclerosant. Heating of the vein and tumescent anesthesia are not required; only local anesthesia is utilized at the insertion site. Previously we showed that endovenous MOCA, using polidocanol, is feasible and safe in the treatment of great spahenous vein (GSV) incompetence. However, larger studies with a prolonged follow-up to prove the efficacy of this technique in terms of obliteration rates are lacking. This randomized trial was designed to compare occlusion rate, post-operative pain and complications between radiofrequency ablation (RFA: the current treatment for GSV incompetence) en MOCA.

NCT ID: NCT01923064 Completed - Portal Hypertension Clinical Trials

Injection of Cyanoacrylate+Lipiodol vs Cyanoacrylate+Lauromacrogol in Gastric Varices

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

The purpose of this randomized study to compare effect of endoscopic injection of a mixture of cyanoacrylate and lipiodol versus cyanoacrylate and lauromacrogol in gastric varices.

NCT ID: NCT01909024 Not yet recruiting - Varicose Veins Clinical Trials

Pelvic Embolisation to Reduce Recurrent Varicose Veins - Recurrent

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

The aim of this study is to identify whether the treatment of pelvic venous reflux (pelvic embolisation) in females with recurrent leg varicose veins, who have a proven contribution to their leg varicose veins from pelvic venous reflux, have a reduction in future recurrence after endovenous laser treatment for recurrent varicose veins in the legs.

NCT ID: NCT01901731 Not yet recruiting - Varicose Veins Clinical Trials

Pelvic Embolisation to Reduce Recurrent Varicose Veins - Primary

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

The aim of this study is to identify whether the treatment of pelvic venous reflux (pelvic coil embolisaton) in females with leg varicose veins, who have a proven contribution to their leg varicose veins from pelvic reflux, have a reduction in recurrence after varicose vein surgery.

NCT ID: NCT01637181 Completed - Varicose Veins Clinical Trials

Clinical Trial of Endovenous 940 and 1470 Laser Ablation for Treating Great Saphenous Veins

COLA
Start date: May 2012
Phase: N/A
Study type: Interventional

A clinical randomized controlled trial, comparing 2 endovenous laser ablation (EVLA) techniques in patients with insufficiency of the great saphenous vein (GSV). There are multiple EVLA devices available, with different wavelengths. In the Netherlands, 940 nm Diode and 1470 nm Nd:Yag laser are the most frequently used devices. Both devices also proven to be equally effective in occluding the GSV. However, little is known about differences in patient-related outcomes. Therefore, the primary outcomes of this comparative clinical trial of 940 nm and 1470 nm EVLA, are pain scores, patient satisfaction and scores of health related and varicose-specific questionnaires. The secondary outcomes are complications and effectiveness of the treatment. It is thought that possibly the 1470 nm ELVA will give lower pain scores and higher patient satisfaction than 940 nm EVLA. No differences are expected in complication rate and effectiveness between the two treatments.

NCT ID: NCT01611324 Completed - Pain Clinical Trials

Painless Local Infiltration Anesthesia

EASE
Start date: May 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess if a dilution with 1.4% sodium bicarbonate of a 2% mepivacaine+epinephrine solution, can be effective in reducing the pain associated with local infiltration anesthesia, during ambulatory phlebectomy procedures.

NCT ID: NCT01508624 Completed - Pain Clinical Trials

Evaluation of Interventions to Improve Pain Relief, Perceived Anxiety and Recovery in Participants Receiving Office Based Surgery

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

This research will evaluate the impact of interventions to improve pain relief and recovery following office based surgery. There will be three phases to this research. The first phase will focus on predicting recovery from office based vein surgery using a multiple regression analysis. Phase two will incorporate a randomised controlled trial to compare the effectiveness of a range of interventions in anxiety and pain reduction and recovery for office based vein surgery patients. The final phase of the investigation will utilise qualitative methodology to explore patients' experiences of each intervention and their opinions about what was and was not effective.

NCT ID: NCT01428076 Completed - Varicose Veins Clinical Trials

Pharmacokinetic Study of Polidocanol Endovenous Microfoam (PEM)

Start date: August 2011
Phase: Phase 1
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 pharmacokinetic profile of two different doses of an investigational drug, Polidocanol Endovenous Microfoam (PEM), an investigational treatment for varicose veins.

NCT ID: NCT01426035 Withdrawn - VARICOSE VEINS Clinical Trials

Safety And Efficacy Study Of Topic Mucopolysaccharide Polysulfate Cream 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 cream in the treatment of superficial varicose veins