A Prospective Outcome Study of Condensed Fenestrated PTFE Mesh (MotifMESH) in Non-sterile Abdominal Wall Defects

Status: Completed
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study will monitor surgically repaired large abdominal hernias requiring condensed fenestrated polytetrafluoroethylene mesh (cPTFE).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: No
View:

• Has a non-sterile abdominal wall defect (incisional hernia or fascial defect) and needs to be repaired

Locations
United States
Illinois
Division of Plastic Surgery
Chicago
Time Frame
Start Date: May 2011
Completion Date: March 2014
Participants
Target number of participants: 10
Treatments
Other: MotifMesh
Condensed polytetrafluoroethylene (cPTFE, MotifMESH) mesh
Related Therapeutic Areas
Sponsors
Leads: Medline Industries

This content was sourced from clinicaltrials.gov

Similar Clinical Trials

We couldn't find any related articles check for more on the main search page.