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May-Thurner Syndrome clinical trials

View clinical trials related to May-Thurner Syndrome.

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NCT ID: NCT02942394 Completed - Clinical trials for Post-thrombotic Syndrome

Treatment of the Postthrombotic Syndrome With the Oblique Stent - TOPOS Study

Start date: December 2016
Phase:
Study type: Observational

Primary objective: To assess the efficacy of the stents (sinus-Obliquus stent for the common iliac vein, the sinus-XL Flex stent or sinus-Venous stent for the external iliac and common femoral veins) by evaluating different gradations of patency rates, patient's rating of disease severity and quality of life in patients with post-thrombotic syndrome and concomitant common iliac vein compression. Secondary objective: To assess long-term safety of venous stenting

NCT ID: NCT02655887 Completed - Clinical trials for Peripheral Vascular Disease

BARD® The VENOVO™ Venous Stent Study for Treatment of Iliofemoral Occlusive Disease

VERNACULAR
Start date: June 15, 2016
Phase: N/A
Study type: Interventional

The BARD® Venovo™ Venous Stent Study is a non-randomized clinical study intended to collect confirmatory evidence of the safety and effectiveness of the Venous Stent for the treatment of iliofemoral occlusive disease.

NCT ID: NCT02584374 Recruiting - Clinical trials for May-thurner Syndrome

Balloon Test for Iliac Vein Compression

Start date: January 2016
Phase: N/A
Study type: Observational

Iliac vein compression is a common cause of leg or abdominal complaints and is difficult to diagnose. Although a combination of duplex ultrasonography, magnetic resonance venography and two-plane phlebography are able to show compression, not all suspected iliac vein compressions can be identified. Intravascular ultrasound appears to have a higher diagnostic value, but is far more expensive. In our experience a balloon occlusion test in the common iliac vein during phlebography can diagnose iliac vein compression due to the collateral network that is visualised. The general consensus is that pelvic collaterals are a sign of pathology, though the investigators would like to validate this test by showing that a balloon occlusion test in healthy subjects does not identify a collateral network.

NCT ID: NCT02240914 Recruiting - Clinical trials for May-Thurner Syndrome

Vascular Ultrasound Versus Intravascular Ultrasound for Diagnosing Iliac Vein Obstruction

USG-DIVO
Start date: February 2013
Phase: N/A
Study type: Observational [Patient Registry]

- Determine the sensitivity, specificity and accuracy of vascular ultrasound, using direct and indirect ultrasonographic signs, in the obstructive diseases of iliac venous segment, in patients with advanced chronic venous insufficiency (CEAP 3-6), considering the intravascular ultrasound (IVUS) as the gold standard for this diagnosis. - Develop an algorithm for noninvasive ultrasound investigation of obstructive lesions in the iliac segment in patients with advanced chronic venous insufficiency (CEAP 3-6).

NCT ID: NCT02149212 Completed - Clinical trials for May-Thurner Syndrome

Iliac Vein Stenting in Advanced Chronic Venous Insufficiency

Start date: February 2013
Phase: Phase 4
Study type: Interventional

About 90 % of vascular symptoms affecting the lower limbs consist of venous diseases. Its highest incidence occurs from the second decade of life, affecting significantly the economically active population. Chronic Venous Insufficiency treatment aims to relieve symptoms, treat and prevent complications, prevent recurrences and provide cosmetic satisfaction with minimal side effects. It's current treatment includes some classic postural measures (leg elevation), elastic stockings and bandages compression therapy and possible medication (phlebotonics). The results in the medium and long term are unfavorable, since a large number of patients do not get better or evolves with recurrence of symptoms. Nowadays many, no prospective , not randomized , international studies have shown favorable results with endovascular treatment of obstruction in the iliac vein territory in patients with advanced Chronic Venous Insufficiency . The purpose of this prospective, double-blinded randomized study is to evaluate the results obtained with endovascular treatment, through the use of angioplasty and stenting in this group of patients when compared with clinical treatment .

NCT ID: NCT01846780 Completed - Clinical trials for Post-thrombotic Syndrome

Treadmill Pilot Study (Invasive Pressure Measurements in PTS)

Start date: December 2013
Phase: N/A
Study type: Observational

Patients with unilateral post-thrombotic obstruction of the iliac tract and or common femoral vein, eligible for stenting are included. Intravenous pressure is measured in both dorsal foot veins and both common femoral veins. Patients are asked to undergo a standardised treadmill test (3.2km/h, 0% slope that increases by 2%/2min, maximum walking time 26 min). Painfree and maximum action radius are noted.

NCT ID: NCT01206751 Completed - Aortic Dissection Clinical Trials

Multi-detector Computer Tomography Protocol Project: Chest Imaging Technique and Case Presentation

Start date: April 2010
Phase: N/A
Study type: Observational

Multi-detector computer tomography protocol project: Chest imaging technique and case presentation.