At a glance
ClinicalIndex Comparison RecordN/ACompleted· 70 enrolled
Drug / intervention
Neo Close Abdominal Closure +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Randomized Trial Evaluating Effectiveness of neoClose Abdominal Closure Device Versus Carter-Thomason Needle Passer
The University of Texas Health Science Center, Houston·interventional·Posted Oct 28, 2015·Updated Aug 28, 2019
In Brief
A clinical study evaluating Neo Close Abdominal Closure and Carter Thomason Device for Surgical Port Site Hernia. Completed, enrolled 70 participants across 1 site.
Detailed Summary
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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSurgical Port Site Hernia
CountriesUnited States
CollaboratorsNeoSurgical Limited
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedOct 2015
Enrollment StartFeb 2016
Primary CompletionApr 2018
TodayJul 2026
First PostedOct 28, 2015
Enrollment StartFeb 12, 2016
Primary CompletionApr 25, 2018
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 10.7 years ago
Interventions
Neo Close Abdominal Closuredevice
Neo Close Abdominal Closure
Carter Thomason Devicedevice
Carter Thomason Device