Same Day Discharge Following Pelvic Reconstructive Surgery
Completed
Conditions studied: Same Day Discharge, Pelvic Organ Prolapse, Total Vaginal Hysterectomy
In brief
This is a prospective cross-sectional study in which patients undergoing major pelvic reconstructive surgery with total vaginal hysterectomy will be recruited and enrolled. At approximately 2 weeks and 12 weeks postoperatively, enrolled patients will be asked to complete a survey detailing their experience with SDD, surgical recovery, and advice for prospective patients.
Key facts
- Study ID
- NCT04804826
- Run by
- TriHealth Inc.
- People needed
- 54
- Starts
- 2021-06-14
- Expected to finish
- 2022-04-06
- Last updated by the study team
- 2024-02-05
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Total vaginal hysterectomy with or without bilateral salpingectomy/oophorectomy
- Apical repair with uterosacral ligament suspension or sacrospinous ligament fixation
- They may also have any of the following concurrent procedures: Anterior repair, Posterior repair, Enterocele repair, Suburethral sling for incontinence
- Surgery by one of the fellowship trained urogynecologists at TriHealth
- English speaking
You may not qualify if…
- Enrollment in the "Diazepam Research Study" (Protocol ID:19-130)
- Concomitant procedure with another surgeon
- Chronic pain conditions that require daily use of narcotic pain medications (including but not limited to: chronic back or pelvic pain, interstitial cystitis, fibromyalgia)
- Concomitant anal sphincteroplasty, mesh removal or use of mesh for prolapse (excluding sling procedures)
Where it is running
- Cincinnati Urogynecology Associates — Cincinnati, Ohio, United States
Full record on ClinicalTrials.gov
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