Trials / Completed
CompletedNCT03526341
Post Market Clinical Follow Up Study for ReliaTack™ Articulating Reloadable Fixation Device With Deep Purchase Tacks
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 116 (actual)
- Sponsor
- Medtronic - MITG · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
A post-market clinical follow-up study for ReliaTack™ articulating reloadable fixation device with deep purchase tacks
Detailed description
A retrospective, multi-center, chart review of medical records on the use of the device for two (2) surgical procedure indications: 1. inguinal/femoral hernia 2. ventral hernia A minimum of 4 sites in the United States will perform chart review and enter 116 study records in the database for data collection. The 116 subject records will be comprised of 76 for the inguinal/femoral indication, and 40 for the ventral indication.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ReliaTack™ Articulating Reloadable Fixation Device | ReliaTack™ Articulating Reloadable Fixation Device with Deep Purchase Tacks |
Timeline
- Start date
- 2018-04-25
- Primary completion
- 2019-09-10
- Completion
- 2019-09-10
- First posted
- 2018-05-16
- Last updated
- 2019-10-09
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03526341. Inclusion in this directory is not an endorsement.