CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 364 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Key inclusion· 4
  • ✓Participant in one of six prior Division of Urogynecology research studies
  • ✓Complete and available postoperative pain scoring data
  • ✓Vaginal reconstructive surgery as primary treatment
  • ✓General anesthesia required
Key exclusion· 2
  • ✕Incomplete or unavailable postoperative pain scoring data
  • ✕Robotic sacrocolpopexy patients excluded

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02996994
NCT02996994N/ACompleted
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Predictors of Postoperative Pain in Urogynecologic Surgery

TriHealth Inc.·observational·Posted Dec 19, 2016·Updated Aug 31, 2023

In Brief

An observational study for Postoperative Pain. Completed, enrolled 364 participants.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsPostoperative Pain
Countries--
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedDec 19, 2016
Enrollment StartDec 1, 2016
Primary CompletionOct 1, 2017
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 9.5 years ago