Prevena Incision Management System Wound Care

Status Terminated

Clinical Trial Summary

Comparison of ventral hernia repair using standard wound care versus Prevena.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02953769
Study type	Observational
Source	Florida Hospital
Contact
Status	Terminated
Phase
Start date	March 29, 2017
Completion date	October 16, 2018

View Details

See also
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