TerminatedNot Applicable

Pelvic Floor Support After Laparoscopic Hysterectomy for Benign Conditions: A Randomized Controlled Trial Comparing Vaginal Cuff Closure Techniques

Stopped: Difficulty with follow up 2/2 COVID-19 Pandemic

United States58 participantsStarted 2017-07-01

Plain-language 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.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Women over 18 years of age undergoing total laparoscopic hysterectomy and robotic assisted total laparoscopic hysterectomy for benign disease. * Subjects must be able to self-consent. * Department of Defense beneficiary Exclusion Criteria: * Patients will be excluded if they undergo a concurrent procedure for prolapse. * If the indication for the procedure is a malignancy. * Those that plan to leave the area in less than 1 year will not be included. * Pop-Q Point C of \>-4

What they're measuring

Pelvic Organ Prolapse - Quantification Point C

Timeframe: 6-8 weeks post op

Pelvic Organ Prolapse - Quantification Point C

Timeframe: 1 year post op

Trial details

NCT IDNCT03753516

SponsorWalter Reed National Military Medical Center

Sponsor typeFED

Study typeINTERVENTIONAL

Primary completion2020-12-30

View on ClinicalTrials.gov More Pelvic Organ Prolapse trials