Overview

Use of a Dual-agent Local Analgesic (Bupivacaine-meloxicam) for Abdominal Incisions in Patients Undergoing Retropubic Mid-urethral Sling Surgery

Status:
Not yet recruiting
Trial end date:
2024-06-01
Target enrollment:
0
Participant gender:
Female
Summary
This study will compare the use of a dual-agent local analgesic (bupivacaine-meloxicam) for abdominal incisions in patients undergoing retropubic mid-urethral sling surgery to see if narcotic usage and pain are impacted.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
TriHealth Inc.
Treatments:
Bupivacaine
Meloxicam
Criteria
Inclusion Criteria:

- undergoing retropubic mid-urethral sling surgery (with concomitant anterior repair or
urethrocele repair)

- English as first language

Exclusion Criteria:

- patients undergoing concomitant posterior repair, vaginal vault suspension, or any
other intra-peritoneal surgeries including hysterectomy

- NSAID use within 7 days of surgery

- steroid use within 10 days

- daily opioid use in the last 3 months

- long acting opioids within 3 days

- any opioids within 24h

- patients unable to consent for themselves

- patients allergic to meloxicam or bupivacaine

- pregnant or lactating patients