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Post Thrombotic Syndrome clinical trials

View clinical trials related to Post Thrombotic Syndrome.

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NCT ID: NCT01637428 Not yet recruiting - Clinical trials for Post Thrombotic Syndrome

The Use of Intermittent Pneumatic Compression Device for Symptomatic Relief in Patients With Post Thrombotic Syndrome

Start date: July 2012
Phase: Phase 2
Study type: Interventional

The use of ActiveCare+S.F.T 3rd generation (an Intermittent Pneumatic Compression Device) will improve quality of life in patients suffering from Post Thrombotic Syndrome compared to compression stockings which is the current gold standard of care.

NCT ID: NCT01615692 Withdrawn - Clinical trials for Deep Vein Thrombosis

The 36-month Extension to Follow up Sub Study

Start date: June 2004
Phase:
Study type: Observational

The purpose of this study is to evaluate leg health for one additional year in patients with symptomatic proximal deep venous thrombosis who did not already develop Post-Thrombotic Syndrome (PTS) during the 2 years of follow up in the SOX Trial.

NCT ID: NCT01578122 Completed - Clinical trials for Deep Vein Thrombosis

Elastic Compression Stockings for Prevention of Post-thrombotic Syndrome

CELEST
Start date: June 29, 2012
Phase: N/A
Study type: Interventional

Post thrombotic syndrome (PTS) is a frequent and burdensome complication of proximal deep-vein thrombosis.Therapeutic options for PTS are limited and mainly rely on its prevention. Therapeutic trials evidenced that elastic compression stockings (ECS) applying 30-40mmHg of pressure at the ankle reduced the rate of PTS by 50%. Although ECS are unlikely to cause harm, in clinical practice, compliance to this treatment appears to be low as ECS may be difficult to apply and to wear. ECS with a lighter compression strength (20-30mmHg) might be easier to apply and be more comfortable. This could favor a better compliance. CELEST is a randomized, multicentre, double-blind trial which aims to determine whether ECS applying 25mmHg of targeted pressure at the ankle are non inferior to ECS applying 35mmHg of targeted pressure at the ankle

NCT ID: NCT01432795 Completed - Clinical trials for Chronic Venous Insufficiency

Practicability of Gliding Aids for Medical Compression Stockings

Start date: November 2010
Phase: Phase 4
Study type: Interventional

Medical compression stockings are highly effective in the prevention, treatment, and secondary prevention of chronic venous insufficiency and of post-thrombotic syndrome. Non-adherence to the prescribed compression treatment concerns approximately 40% of patients. Elderly patients are often unable to handle stockings in order to put them on properly in the morning and to undress in the evening. Gliding aids and stocking "butlers" are two types of tools to facilitate the dressing manoeuvre with medical stockings. The present study evaluates four different gliding aids and two different stocking "butlers" to put on three different types of compression stockings. The study is conducted with forty consenting subjects with advanced chronic venous insufficiency.

NCT ID: NCT00858130 Completed - Clinical trials for Deep Vein Thrombosis

Pilot Study for VeinoPlus to Improve Symptoms of Postthrombotic Syndrome (PTS)

VeinoPlus
Start date: March 2009
Phase: N/A
Study type: Interventional

The investigators plan to perform an exploratory study to investigate the effects of electro-stimulation of the legs on the symptoms and clinical findings of post thrombotic syndrome (PTS), as well as quality of life of patients with PTS. The investigators theorize that electro-stimulation will provide both a mechanical benefit via muscular contraction and increased venous outflow from the affected extremity, as well as an anesthetic effect, which the investigators anticipate will translate into improved symptomatic outcomes, quality of life (QOL) benefits.

NCT ID: NCT00790335 Completed - Clinical trials for Venous Thromboembolism

Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis

ATTRACT
Start date: November 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the use of adjunctive Pharmacomechanical Catheter Directed Thrombolysis, which includes the intrathrombus administration of rt-PA--Activase (Alteplase),can prevent the post-thrombotic syndrome(PTS)in patients with symptomatic proximal deep vein thrombosis(DVT)as compared with optimal standard DVT therapy alone.

NCT ID: NCT00633971 Completed - Clinical trials for Post Thrombotic Syndrome

Treatment Trial for Post-Thrombotic Syndrome

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if complex lymphedema therapy is effective in decreasing disease severity and improving quality of life in patients with post thrombotic syndrome.