The neoClose Abdominal Closure vs Carter-Thomason Trial
Completed · Not applicable
Conditions studied: Surgical Port Site Hernia
In brief
The purpose of this study is to compare the neoClose abdominal closure to the standard Carter-Thomason closure in a bariatric surgery gastric bypass population.
Key facts
- Study ID
- NCT02589171
- Run by
- The University of Texas Health Science Center, Houston
- People needed
- 70
- Starts
- 2016-02-12
- Expected to finish
- 2018-04-25
- Last updated by the study team
- 2019-08-28
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Morbid obesity (BMI > 35).
- Completed multimodality pre operative evaluation (Psychology, Nutrition, Support Groups).
- Approved for robotic assisted laparoscopic gastric bypass.
You may not qualify if…
- Previous midline laparotomy or weight loss procedure.
Where it is running
- The University of Texas Health Science Center at Houston — Houston, Texas, United States
Full record on ClinicalTrials.gov
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