Registry for patients with deep venous obstructions

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This ongoing registry collects data on patients suffering from deep venous obstructive disease who are treated using percutaneous transluminal angioplasty (PTA) and stenting, with or without surgical desobstruction of the common femoral vein. The study aims to document the effectiveness and safety of these interventions in patients with significant symptoms and confirmed venous obstruction through imaging techniques. The data is continuously updated in a digital database at a tertiary medical center, allowing for real-time analysis and insights into treatment outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Venous obstruction/occlusion in the femoral vein, common femoral vein, external iliac vein, common iliac vein or inferior vena cava

Exclusion Criteria:

* Intolerance to anticoagulant medication
* A life expectancy \<1 year

Where it's running

• Maastricht University Medical Centre
  Maastricht, Netherlands Recruiting

Study contacts

• Principal investigator: Cees Wittens, MD, PhD — Maastricht University Medical Centre
• Study coordinator: Mark A de Wolf, MD
• Email: m.dewolf@maastrichtuniversity.nl

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.