Trials / Withdrawn
WithdrawnNCT00668681
Evaluation of EndoRefix Endovascular Delivery System and Staple
Safety Data Collection for Delivery System and Use of Staple in Endovascular Procedures
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Lombard Medical · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
This study is intended to provide data to verify safe delivery of a staple previously intended for use in open surgical procedures. A newly modified delivery system will provide endovascular access for implantation of a staple during endovascular graft procedures.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | EndoRefix |
Timeline
- Start date
- 2008-04-01
- Primary completion
- 2008-12-01
- Completion
- 2009-02-01
- First posted
- 2008-04-29
- Last updated
- 2012-10-17
Locations
7 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00668681. Inclusion in this directory is not an endorsement.