Safety Study of MotifMESH (cPTFE) in Abdominal Surgery
NCT01364233 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10
Last updated 2019-02-26
Summary
This study will monitor surgically repaired large abdominal hernias requiring condensed fenestrated polytetrafluoroethylene mesh (cPTFE).
Conditions
- Hernia
Interventions
- DEVICE
-
MotifMESH
Polytetrafluoroethylene (cPTFE) macroporous mesh
Sponsors & Collaborators
-
Medline Industries
lead INDUSTRY
Principal Investigators
-
Gregory A Dumanian, MD · Northwestern University
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-05-31
- Primary Completion
- 2014-03-31
- Completion
- 2014-03-31
Countries
- United States
Study Locations
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