FRAMED Infrainguinal Venous Bypass Versus Conventional Autologous Bypass Trial
Recruiting
N/A
Interventional Study
Peripheral Arterial Occlusive Disease
Femoropopliteal Artery Occlusion
Femoropopliteal Stenosis
Critical Limb-Threatening Ischemia
Claudication, Intermittent
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 110 (estimated)
- Sponsor
- Paracelsus Medical University · Other
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About This Trial
The purpose of this clinical trial is to analyze patency after autologous infrainguinal bypass surgery in patients receiving a venous conduit versus a covered venous conduit.
Trial Locations
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Eligibility Criteria
Inclusion Criteria
* Age at least 18 years
* Informed consent form with signature
* Rutherford Category 3 (\<200m) or chronic critical ischemia (Rutherford Category 4-6)
* Assured inflow and recipient artery.
Exclusion Criteria
* Pregnant or breastfeeding women
* Active infection or sepsis
* Acut…
Contacts