Trials / Terminated
TerminatedNCT02953769
Prevena Incision Management System Wound Care
Use of Prevena Incision Management System in Wound Morbidity in Complex Ventral Hernia Patients. A Prospective Randomized Control Trial
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 61 (actual)
- Sponsor
- AdventHealth · Academic / Other
- Sex
- All
- Age
- 18 Years – 89 Years
- Healthy volunteers
- Not accepted
Summary
Comparison of ventral hernia repair using standard wound care versus Prevena.
Detailed description
Compare the outcomes for patients who have abdominal reconstruction for ventral hernia repair, regarding wound morbidity, post-operative pain and patient comfort to ambulation, with the use of Prevena™ to those patients who have ventral hernia repair to those who have standard wound care.
Conditions
Timeline
- Start date
- 2017-03-29
- Primary completion
- 2018-10-16
- Completion
- 2018-10-16
- First posted
- 2016-11-03
- Last updated
- 2019-08-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02953769. Inclusion in this directory is not an endorsement.