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Venous Insufficiency clinical trials

View clinical trials related to Venous Insufficiency.

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NCT ID: NCT01509599 Completed - Clinical trials for Venous Insufficiency

Cooling Lower Leg Skin to Prevent Venous Leg Ulcers in Patients With Poor Vein Circulation

Start date: August 2011
Phase: Phase 1/Phase 2
Study type: Interventional

Leg vein circulation problems can damage the skin of the lower legs, especially around the ankles, by making it discolored, hard, itchy, red, and swollen. Ulcers often develop. Inflammation is often present in the damaged skin. This study will test whether using a special low compression, cooling, boot-like gel wrap placed around the damaged skin of the lower legs will improve the skin circulation and prevent leg ulcers. The study hypothesis is: A cryotherapy, low-compression cooling gel wrap (CW) plus usual care (UC) (leg elevation, compression stockings) intervention compared to a low compression non-cryotherapy "sham" wrap (NW) plus UC will reduce tissue blood flow (perfusion units) and decrease the incidence of venous leg ulcers (VLUs) during the 9-month study period in individuals with Stage 4 and 5 venous insufficiency.

NCT ID: NCT01501188 Completed - Clinical trials for Chronic Venous Insufficiency

Efficacy Study of Kinesio Taping to Treat Muscular and Joint Problems in Chronic Venous Insufficiency

Start date: September 2008
Phase: Phase 1
Study type: Interventional

The purpose of this study is to analyze the effects of Kinesio Taping on gastrocnemius muscle activation during gait and on Range of ankle motion in postmenopausal females with Chronic Venous Insufficiency in initial stages in comparison to a placebo control group.

NCT ID: NCT01477281 Not yet recruiting - Clinical trials for Chronic Venous Insufficiency

Study to Evaluate the Efficacy and Tolerability of Venaflon Use in Reducing the Symptoms Caused by Chronic Venous Insufficiency When Compared With Daflon

Start date: February 2012
Phase: Phase 3
Study type: Interventional

The objective is to evaluate the effectiveness of the safety of Daflon in decreasing symptoms resulting from chronic venous insufficiency when compared with Daflon.

NCT ID: NCT01458795 Completed - Clinical trials for Venous Insufficiency

The Fate Of Calf Perforators After Endovenous Laser Ablation Of Saphenous Veins

Start date: n/a
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the morphologic and hemodynamic changes in the calf perforators after endovenous laser ablation of saphenous veins.

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: NCT01425554 Completed - Clinical trials for Chronic Cerebrospinal Venous Insufficiency

Doppler Sonography, MR Venography, Plethysmography for the Diagnosis of CCSVI

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

This study is aimed at evaluation of diagnostic value of Doppler sonography, MR venography and air-plethysmography for the assessment of abnormalities in the internal jugular veins, with catheter venography as the reference test.

NCT ID: NCT01415622 Completed - Clinical trials for Venous Insufficiency

Feasibility, Efficacy, and Safety of Venous Ulcer Treatment Using a Hand Plasma Generator (PlasmaDerm) Chronisch venöser Ulzerationen (PlasmaDerm)

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

The purpose of this study is to prove the safety and efficacy of plasma as an add-on treatment in combination with conventional treatment in cases of chronical venous Ulcus cruris.

NCT ID: NCT01402921 Completed - Clinical trials for Chronic Venous Insufficiency (CVI)

Efficacy on Volume Reduction and Tolerance of Progressiv' Medical Compressive Therapy (MCT) V0322 BC in Patients With Chronic Venous Oedema

Start date: January 2011
Phase: Phase 3
Study type: Interventional

Elastic MCT is a widely recognized and the consensus-approved treatment for chronic venous insufficiency (CVI).Efficacy evidence level is often insufficient (grade B or C), or based on studies carried prior to CEAP classification (2004). Item C3 of this classification relates to patients suffering from chronic venous disease and permanent oedema. Literature mentions only one study in which volume reduction in venous-induced oedema was primary endpoint. Indeed, 240 patients showed a 46.7 ± 8.2 ml reduction (SEM) after 12 weeks with a Class 2 compression sock (15-20 mm Hg at ankle). Volume is an accurate and reproducible quantitative measure considered nowadays as being gold standard when objectifying oedema variation. It is therefore particularly relevant in a C3-patient trial (CEAP classification). The main objective of the current study is to evaluate the clinical effect of Progressiv' MCT on volume reduction in permanent CVI-oedema after 3 months of treatment.

NCT ID: NCT01372020 Completed - Clinical trials for Chronic Venous Insufficiency

Neuromuscular Electrical Therapy in Venous Ulcers

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

The use of neuromuscular electrical stimulation in the treatment of venous ulcers with difficulty of repair could be an alternative therapeutic favoring devitalized tissues and hence the pain. The aim of this study is to evaluate the effect of neuromuscular electrical stimulation on pain and area of venous ulcers in patients with venous insufficiency.

NCT ID: NCT01371760 Completed - Multiple Sclerosis Clinical Trials

BRAVE-DREAMS (BRAin VEnous DRainage Exploited Against Multiple Sclerosis)

BRAVE-DREAMS
Start date: August 2012
Phase: N/A
Study type: Interventional

To assess in a double blinded randomized control trial (RCT) study design safety and effectiveness of balloon angioplasty of the main extracranial and extravertebral veins in multiple sclerosis (MS) associated to chronic cerebrospinal venous insufficiency (CCSVI). Mean follow-up 1 year. 5-8 Italian centres 360 relapsing remitting (RR) MS patients will be randomized, with expanded disability disease scale (EDSS) ranging 2-5.5, age 18-65.