Trials / Completed
CompletedNCT01863030
A Prospective, Observational Study Utilizing Phasix™ Mesh During Ventral and Incisional Hernia Repair Surgery
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 31 (actual)
- Sponsor
- John Roth · Academic / Other
- Sex
- All
- Age
- 18 Years – 100 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to collect efficacy, safety and utility data with Phasix™ Mesh in ventral and incisional repair procedures by evaluating the following: 1. Hernia recurrence rate of ventral and incisional hernias post repair with Phasix™ Mesh for up to 12 months post surgery. 2. Perioperative, short-term and long-term procedural and/or device related complications. 3. Abdominal Wall Function and mobility.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Phasix mesh implant |
Timeline
- Start date
- 2013-05-01
- Primary completion
- 2016-11-01
- Completion
- 2016-11-01
- First posted
- 2013-05-27
- Last updated
- 2020-01-21
- Results posted
- 2020-01-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01863030. Inclusion in this directory is not an endorsement.