Trials / Unknown
UnknownNCT05400083
Prevention of Incisional Hernia With Biosynthetic Mesh at the Site of Temporary Ileostomy Closure (PRINCESS)
Prevention of Incisional Hernia With Biosynthetic Mesh at the Site of Temporary Ileostomy Closure
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 203 (estimated)
- Sponsor
- Federico II University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- —
Summary
Prophylactic mesh reinforcement of the abdominal wall at the site of temporary ileostomy closure is effective in preventing postoperative incisional hernia. This prospective, multicenter, observational study will evaluate performance of Phasix biosynthetic mesh when used to reinforce fascial closure .
Conditions
Timeline
- Start date
- 2021-05-17
- Primary completion
- 2023-05-01
- Completion
- 2024-05-01
- First posted
- 2022-06-01
- Last updated
- 2022-06-03
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT05400083. Inclusion in this directory is not an endorsement.