At a glance
ClinicalIndex Comparison RecordN/ACompleted· 79 enrolled
Drug / intervention
EZ close +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.
Single Blind Randomized Control Trial Evaluating Efficacy and Safety of EZ-Close Port-site Closure Device Versus Carter-Thomason Device
In Brief
A clinical study evaluating EZ close and Carter Thomason for Surgical Port Site Hernia. Completed, enrolled 79 participants across 1 site.
Detailed Summary
This study aims to evaluate the efficacy and safety of a novel port-site closure device (EZ Close) by comparing it with the Carter-Thomason device.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSurgical Port Site Hernia
CountriesSouth Korea
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartAug 2017
First PostedDec 2017
Primary CompletionMay 2018
Study CompletionMay 2018
TodayJul 2026
First PostedDec 15, 2017
Enrollment StartAug 17, 2017
Primary CompletionMay 9, 2018
Study CompletionMay 24, 2018
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 8.5 years ago
Interventions
EZ closedevice
EZ close used.
Carter Thomasondevice
Carter Thomason used.