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NCT02156687 · ClinicalTrials.gov registry record · NA
Randomized Trial of Y Mesh vs Dual Mesh
A NA study of Prolapse, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 59
- Enrollment target
- 1
- Study location
NCT02156687 is a NA study of Prolapse that has completed, run by The Cleveland Clinic. The registered enrollment target is 59 participants, below the 230-participant average among 3 other Prolapse trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02156687, a NA study of Prolapse, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 59 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- DEVICE Y mesh
- DEVICE Dual flat mesh
Study Locations (1)
Ohio
- Cleveland Clinic - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 59 participants |
| Start Date | 2014-04-14 |
| Est. Completion | 2020-04-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02156687
The ClinicalTrials.gov registry entry for NCT02156687 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 59 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 230-participant average among 3 other Prolapse trials with a reported enrollment target (74% lower). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Prolapse appearing as the primary indexed condition, and to 2 interventions - of which Y mesh is the first listed.
NCT02156687 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT02156687 about?
NCT02156687 is a clinical study titled "Randomized Trial of Y Mesh vs Dual Mesh". 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 ...
What is the current status of trial NCT02156687?
This trial is currently completed. It is a NA study. The enrollment target is 59 participants. The study started on 2014-04-14. Estimated completion is 2020-04-01.
What conditions does trial NCT02156687 study?
This clinical trial studies the following conditions: Prolapse.
What interventions are being tested in trial NCT02156687?
The interventions under investigation include: Y mesh (DEVICE), Dual flat mesh (DEVICE).
Who is sponsoring clinical trial NCT02156687?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02156687 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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