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Dacron vs Dardik for Fem-Pop Bypass

NCT00523263 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL

Last updated 2007-08-31

No results posted yet for this study

Summary

Clinical trial for the comparison of long-term patency of heparin-bonded Dacron and human umbilical vein vascular prostheses in above-knee femoro-popliteal bypass surgery.

Conditions

  • Intermittent Claudication
  • Arterial Occlusive Diseases
  • Atheroslerosis

Interventions

DEVICE

heparin-bonded and collagen coated polyster

femoro-popliteal bypass

DEVICE

Human umbilical vein femoro-popliteal bypass

Sponsors & Collaborators

  • Radboud University Medical Center

    lead OTHER

Principal Investigators

  • J. Adam van der Vliet, MD, PhD · Radboud University Medical Center Nijmegen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
31 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1996-01-31
Completion
2007-04-30

Countries

  • Netherlands

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 NCT00523263 on ClinicalTrials.gov