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Not Yet Recruiting
NCT07842159
Long-acting Local Vaginal Cuff Anesthesia Following Hysterectomy
Conditions: Pain, Postoperative
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE1, PHASE2
Enrollment: 104
Sponsor: The University of Texas Health Science Center, Houston
Location: The University of Texas Health Science Center, Houston Houston Texas
Summary
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.
Eligibility Criteria
Inclusion Criteria:
* at least 66.5kg weight
* elective Robotic assisted (RA) Total Laparoscopic Hysterectomy (TLH) for benign indications at Memorial Hermann Hospital Texas Medical Center, Memorial Hermann Hospital Cypress and Memorial Hermann Hospital Greater Heights.
Exclusion Criteria:
* Combined operation or alternative approach
* inpatient overnight admission
Source: ClinicalTrials.gov (NCT07842159). StuddyBuddy aggregates publicly available trial information.
