Not recruiting yet
Long-acting Local Vaginal Cuff Anesthesia Following Hysterectomy
NCT07842159 · The University of Texas Health Science Center, Houston · Updated 25 Sept 2026
- What is being tested
- Combined Bupivacaine and Exparel; Normal Saline (NS)
- For
- Pain, Postoperative
- Kind of study
- Tests a treatment or device on volunteers. Phase 1 and Phase 2.
- Who can join
- Ages 18 years and older. About 104 people. The full rules are on the registry page.
- Where
- United States
- When
- Starts or started 17 Sept 2026, ends 15 Sept 2028. Registered 25 Sept 2026.
- Results
- None posted yet.
In the researchers' words
The purpose of this study is to compare recovery unit and post operation day (POD) 1 pain score in women following elective robotic assisted TLH (RA-TLH) for benign indication with and without local vaginal cuff injection of short acting bupivacaine and long acting Exparel, to evaluate postoperative pain management and control by assessing the amount and frequency of NSAIDS and opioids taken and to assess bleeding, vaginal discharge and or vaginal dehiscence at the postoperative follow up visit.
Sites
- The University of Texas Health Science Center, HoustonHouston, Texas, United States
