PREPARE: Perioperative REhabilitation Around Vaginal Prolapse RepAir Surgery for Recovery Enhancement
Recruiting
N/A
Interventional Study
Postoperative Physical Functioning
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 56 (estimated)
- Sponsor
- University of New Mexico · Other
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About This Trial
Pelvic organ prolapse is a common problem faced by millions of patients in the United States, leading to an estimated 200,000 surgeries per year. The majority of patients in the US undergoing vaginal suspension between the ages of 60-79. Deconditioning and decreased functional status after surgery can be more pronounced in elderly populations. It is important to explore ways to improve postoperati…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Subjects are ≥ 18 years of age
* English or Spanish speaking
* Stage 2, 3 or 4 uterovaginal or vaginal vault prolapse.
* Patient scheduled to undergo transvaginal sacrospinous ligament suspension, uterosacral ligament suspension, or Manchester procedure at The University of Ne…
Contacts