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Multicenter Assessment of the Safety and Efficacy of the Minnow Medical GRST™ Peripheral Catheter System

NCT00881257 · Status: TERMINATED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2013-06-20

No results posted yet for this study

Summary

The objective of this clinical investigation is to evaluate the safety and efficacy of the Minnow Medical GRST™ Peripheral Catheter System in the treatment of de novo lesions in the superficial femoral artery (SFA) or the popliteal artery.

Conditions

  • Peripheral Vascular Disease

Interventions

DEVICE

GRST Peripheral Catheter System

Treatment to dilate stenoses and reduce plaque in treated vessels

Sponsors & Collaborators

  • Vessix Vascular, Inc

    lead INDUSTRY

Principal Investigators

  • Hans Krankenberg, MD · Hamburg University Cardiovascular Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-08-31
Primary Completion
2009-11-30
Completion
2010-05-31

Countries

  • Germany

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 NCT00881257 on ClinicalTrials.gov