Trials / Terminated
TerminatedNCT01984996
Freedom Inguinal Hernia Repair System Study
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- Insightra Medical, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of this study is to evaluate patient quality-of-life (QOL) after inguinal hernia repair. "Carolinas Comfort Scale" (CCS) assessments will be held at regular intervals. The secondary objective of the study is to follow short-term and long-term study-related complications/adverse events.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Freedom ProFlor Inguinal Hernia Implant |
Timeline
- Start date
- 2013-12-01
- Primary completion
- 2017-12-01
- First posted
- 2013-11-15
- Last updated
- 2016-06-09
Locations
8 sites across 3 countries: United States, Austria, Italy
Source: ClinicalTrials.gov record NCT01984996. Inclusion in this directory is not an endorsement.