Trials / Completed
CompletedNCT02500537
A Post-market Study of the Endo GIA™ Reinforced Reload With Tri-Staple™ Technology
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Medtronic - MITG · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
A post-market study of the Endo GIA™ Reinforced Reload with Tri-Staple™ Technology.
Detailed description
The objective of this prospective, two-arm, multicenter, post-market study is to evaluate safety through the incidence of reported device-related adverse events (AEs) through 30 days following use of the Endo GIA™ Reinforced Reload with Tri-Staple™ Technology in subjects undergoing indicated abdominal or thoracic procedures.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Endo GIA™ Reinforced Reload with Tri-Staple™ Technology | Endo GIA™ Reinforced Reload with Tri-Staple™ Technology (Universal Handle) |
Timeline
- Start date
- 2015-05-01
- Primary completion
- 2016-05-01
- Completion
- 2016-08-01
- First posted
- 2015-07-16
- Last updated
- 2017-04-04
- Results posted
- 2017-04-04
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT02500537. Inclusion in this directory is not an endorsement.