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Study identifier: NCT05979493 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

QL Block in Laparoscopic Myomectomy

Condition: Postoperative Pain · Fibroid Uterus  ·  Sponsor: Joseph Findley MD

PhasePhase 4
Planned participants80
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Catherine P Haering, BA  ·  3392011531  ·  cph43@case.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospitals Ahuja Medical CenterBeachwood, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05979493