OncoMatch/Clinical Trials/NCT05979493
QL Block in Laparoscopic Myomectomy
Is NCT05979493 recruiting? Yes, currently enrolling (May 2026). This Phase 4 trial studies multiple treatments including Bupivacain and Saline for postoperative pain.
Treatment: Bupivacain · Saline — This study aims to determine the efficacy of a quadratus lumborum (QL) block in decreasing postoperative pain in patients undergoing myomectomy for uterine fibroids. A QL block is a temporary anesthetic injection in the quadratus lumborum muscle, a muscle in the lower back, that has been previously shown to significantly reduce postoperative pain levels in patients undergoing abdominal and pelvic surgery. Because of its demonstrated effects, the QL block is becoming a standard of anesthesia and surgical care. Since participants will be undergoing a myomectomy procedure, the investigators believe that participants may qualify to participate in this study. The investigators will be comparing patients who receive the QL block (in addition to standard anesthesia and postoperative pain care) with patients who do not receive the QL block (in addition to standard care). The participants will be randomly assigned to one of the two groups and may or may not actually receive the block.
Check if I qualifyEligibility summary
For patients with Uterine Leiomyoma.
This summary was generated by AI from the trial's official eligibility criteria and may contain errors. Always confirm with the study team before contacting a site.
US trial sites
- University Hospitals Ahuja Medical Center · Beachwood, Ohio
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