Evaluation of the GORE® C3 Delivery System Module

NCT01398332 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 399

Last updated 2024-08-01

No results posted yet for this study

Summary

This is an observational Registry designed to obtain early data on the use of the GORE® EXCLUDER® AAA Endoprosthesis with C3 Delivery System.

Conditions

  • Aortic Aneurysm, Abdominal

Interventions

DEVICE

Stent graft (EXCLUDER)

Endovascular repair

Sponsors & Collaborators

  • W.L.Gore & Associates

    lead INDUSTRY

Principal Investigators

  • Eric Verhoeven, MD · Klinikum Nürnberg-Süd

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2024-07-31
Completion
2024-07-31

Countries

  • Germany

Study Locations

More Related Trials

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 NCT01398332 on ClinicalTrials.gov