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Graft-Augmented Rectocele Repair-A Randomized Surgical Trial
Providence, RI
N/A
Waitlist Available
Led By Vivian W Sung, MD MPH
Research Sponsored by Women and Infants Hospital of Rhode Island
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
The purpose of this study is to determine whether adding a graft during a rectocele repair will improve the success rate of the repair.
Eligible Conditions
- Rectocele
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: 2Experimental Treatment1 Intervention
Posterior repair with graft
Group II: 1Active Control1 Intervention
Native tissue repair
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Graft augmented posterior repair
2004
N/A
~160
Find a Location
Closest Location:Women and Infants Hospital of Rhode Island· Providence, RI
Who is running the clinical trial?
Women and Infants Hospital of Rhode IslandLead Sponsor
118 Previous Clinical Trials
59,120 Total Patients Enrolled
Vivian W Sung, MD MPHPrincipal InvestigatorWomen and Infants Hospital