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Multicentric, Prospective, Randomized, Comparing Trial Between Bypass of the Femoropoplitea by PTFE and Heparin Bounded PTFE

NCT00147979 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 596

Last updated 2014-12-05

No results posted yet for this study

Summary

Comparison of two kinds of protheses for bridging of the femoropoplitea and/or femorotibiale: PTFE with or without bounded heparin

Conditions

  • Peripheral Vascular Diseases

Interventions

DEVICE

Bridging by PTFE with bounded heparin

Bridging by PTFE with bounded heparin

DEVICE

Bridging by PTFE without bounded heparin

Bridging by PTFE without bounded heparin

Sponsors & Collaborators

  • JOTEC Company

    collaborator OTHER

  • University Hospital, Ghent

    lead OTHER

Principal Investigators

  • Frank Vermassen, MD, PhD · University Hospital, Ghent

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-04-30
Primary Completion
2009-01-31
Completion
2013-08-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00147979 on ClinicalTrials.gov