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Vaginal - Vaginal Cuff Closure for Pelvic Organ Prolapse

N/A
Waitlist Available
Research Sponsored by Walter Reed National Military Medical Center
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 6-8 weeks post op
Awards & highlights
No Placebo-Only Group

Summary

The purpose of this study is to learn about the effect of different vaginal cuff closure techniques on pelvic support after laparoscopic hysterectomy and robotic assisted laparoscopic hysterectomy for benign gynecologic conditions.

Eligible Conditions
  • Pelvic Organ Prolapse

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6-8 weeks post op
This trial's timeline: 3 weeks for screening, Varies for treatment, and 6-8 weeks post op for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Pelvic Organ Prolapse - Quantification Point C

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Active Control
Group I: Vaginal - Vaginal Cuff ClosureActive Control1 Intervention
Group II: Laparoscopic - Vaginal Cuff ClosureActive Control1 Intervention

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Who is running the clinical trial?

Walter Reed National Military Medical CenterLead Sponsor
140 Previous Clinical Trials
33,115 Total Patients Enrolled
1 Trials studying Pelvic Organ Prolapse
138 Patients Enrolled for Pelvic Organ Prolapse
~7 spots leftby Dec 2025
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