Clinical Trials Directory

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UnknownNCT01698671

InterGard Synergy Post-Marketing Surveillance Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Maquet Cardiovascular · Industry
Sex
All
Age
—
Healthy volunteers
Not accepted

Summary

The purpose of the study is to assess the performance and safety of the InterGard Synergy vascular graft.

Detailed description

Study of the device in patients with aneurysmal and occlusive disease of the abdominal aorta and peripheral arteries.

Conditions

Interventions

TypeNameDescription
DEVICEInterGard Synergy Vascular Graft

Timeline

Start date
2012-10-01
Primary completion
2013-10-01
Completion
2014-05-01
First posted
2012-10-03
Last updated
2013-11-26

Locations

3 sites across 2 countries: Austria, Germany

Source: ClinicalTrials.gov record NCT01698671. Inclusion in this directory is not an endorsement.

InterGard Synergy Post-Marketing Surveillance Study (NCT01698671) · Clinical Trials Directory