N/A
N=364
Predictors of Postoperative Pain
Postoperative Pain
Bottom Line
View on ClinicalTrials.gov: NCT02996994 ↗Enrolled (actual)
364
Serious AEs
0.0%
Results posted
Aug 2023
Primary outcome: Primary: Visual Analog Scale (VAS) Pain Score — 38.16 mm
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Female
- Sponsor
- TriHealth Inc.
- Primary completion
- Oct 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Visual Analog Scale (VAS) Pain Score |
38.16 | — |
Summary
This is a retrospective chart review using TriHealth Electronic Privacy Identification Center (EPIC) and previously developed databases for TriHealth Institutional Review Board (IRB) approved research studies within the Division of Urogynecology and Reconstructive Pelvic Surgery to determine the predictors of postoperative pain specific to the urogynecologic patient population.
Eligibility Criteria
Inclusion Criteria
- Participant in one of six research studies previously performed by the Division of Urogynecology and Pelvic Reconstructive Surgery (#13090, #13072, #12136, #12132, #10072, or #09001)
- Postoperative pain scoring data complete and available
- Vaginal reconstructive surgery as primary treatment
- General anesthesia
Exclusion Criteria
- Incomplete or unavailable postoperative pain scoring
- Robotic sacrocolpopexy patients will be excluded
Data sourced from ClinicalTrials.gov (NCT02996994). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.