At a glance
ClinicalIndex Comparison RecordN/ACompleted· 59 enrolled
Drug / intervention
Y mesh +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.
A Prospective Randomized Trial Comparing Restorelle Y Mesh vs. Restorelle Dual Flat Mesh for Laparoscopic and Robotic-assisted Laparoscopic Sacrocolpopexy
In Brief
A clinical study evaluating Y mesh and Dual flat mesh for Prolapse. Completed, enrolled 59 participants across 1 site.
Detailed Summary
The primary objective of the proposed study is to determine the difference in suturing time when using the restorelle Y mesh versus the restorelle dual flat mesh at the time of laparoscopic and robotic-assisted laparoscopic sacrocolpopexy. Hypothesis: Suturing time when using the restorelle Y mesh will be faster than when using the restorelle dual flat mesh at the time of laparoscopic and robotic-assisted laparoscopic sacrocolpopexy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsProlapse
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
Enrollment StartApr 2014
First PostedJun 2014
Primary CompletionNov 2019
Study CompletionApr 2020
TodayJul 2026
First PostedJun 5, 2014
Enrollment StartApr 14, 2014
Primary CompletionNov 7, 2019
Study CompletionApr 1, 2020
TodayJul 2, 2026
Enrollment to primary: 5.6 yearsPosted 12.1 years ago
Interventions
Y meshdevice
Y mesh
Dual flat meshdevice
Dual flat mesh