Status:
RECRUITING
Paracervical Injection and Opioid Use After Vaginal Hysterectomy for Prolapse
Lead Sponsor:
University of North Carolina, Chapel Hill
Conditions:
Opioid Use
Surgical Recovery
Eligibility:
FEMALE
18+ years
Phase:
PHASE4
Brief Summary
The goal of the study to see if giving a numbing medicine around the cervix (called a paracervical block) during vaginal hysterectomy with prolapse repair helps people feel less pain and need fewer st...
Detailed Description
Secondary outcomes are to: 1. Compare postoperative pain scores in patients undergoing vaginal hysterectomy for prolapse repair who receive an intraoperative paracervical block compared to placebo 2....
Eligibility Criteria
Inclusion
- Individuals undergoing vaginal hysterectomy with concomitant prolapse repair procedure
Exclusion
- Non-English speaking
- Weight less than 50 kg
- Allergy to bupivacaine
- Pregnant
Key Trial Info
Start Date :
October 20 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2026
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT07213635
Start Date
October 20 2025
End Date
December 1 2026
Last Update
October 24 2025
Active Locations (1)
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1
University of North Carolina Urogynecology and Reconstructive Pelvic Surgery at REX
Raleigh, North Carolina, United States, 27607