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NCT02696239 · ClinicalTrials.gov registry record · NA
Vaginal Cuff Closure in Robotic Hysterectomy
A NA study of Complications of Medical Care, sponsored by Henry Ford Health System.
- Completed
- Registry status
- NA
- Development phase
- 90
- Enrollment target
- 1
- Study location
NCT02696239 is a NA study of Complications of Medical Care that has completed, run by Henry Ford Health System. The registered enrollment target is 90 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02696239, a NA study of Complications of Medical Care, has completed, sponsored by Henry Ford Health System.
- COMPLETED
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to evaluate the impact of implementing different types of suturing materials and techniques of vaginal cuff closure in robotic assisted laparoscopic hysterectomy on cost, operative time and post operative surgical outcomes.
Conditions Studied
Interventions
- DEVICE V-lock suture
- DEVICE Vicryl Suture
- DEVICE Lapra-Ty II
Study Locations (1)
Michigan
- Henry Ford Hospital - Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2010-09 |
| Est. Completion | 2016-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02696239
The ClinicalTrials.gov registry entry for NCT02696239 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Complications of Medical Care appearing as the primary indexed condition, and to 3 interventions - of which V-lock suture is the first listed.
NCT02696239 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.
Frequently Asked Questions
What is clinical trial NCT02696239 about?
NCT02696239 is a clinical study titled "Vaginal Cuff Closure in Robotic Hysterectomy". The purpose of this study is to evaluate the impact of implementing different types of suturing materials and techniques of vaginal cuff closure in robotic assisted laparoscopic hysterectomy on cost, operative time and post operative surgical outcomes.
What is the current status of trial NCT02696239?
This trial is currently completed. It is a NA study. The enrollment target is 90 participants. The study started on 2010-09. Estimated completion is 2016-02.
What conditions does trial NCT02696239 study?
This clinical trial studies the following conditions: Complications of Medical Care.
What interventions are being tested in trial NCT02696239?
The interventions under investigation include: V-lock suture (DEVICE), Vicryl Suture (DEVICE), Lapra-Ty II (DEVICE).
Who is sponsoring clinical trial NCT02696239?
This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02696239 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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