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Completed NCT07705516

Interfascial Abdominal Wall Block for Gynecological Laparoskopy: A Randomized Clinical Trial

Conditions: Postoperative Pain, Pelvic Pain

Sex: Female
Ages: 25 Years – 65 Years
Healthy volunteers: No
Phase: NA
Enrollment: 50
Sponsor: Medical and Diagnostic Center "MEDION" LLC

Location: Medical and Diagnostic Center "MEDION" LLC Poltava Poltava Oblast

Summary

The purpose of this study is to evaluate the clinical efficacy of combining ultrasound-guided bilateral rectus sheath blocks (RSB) and quadratus lumborum blocks (QLB) compared to using a quadratus lumborum block alone for postoperative analgesia in patients undergoing laparoscopic gynecological surgeries. The primary objective is to assess movement-evoked pain scores in the early postoperative period. Secondary objectives include the evaluation of postoperative opioid consumption, intraoperative hemodynamic stability, and the overall incidence of side effects. Investigators hypothesize that the combined interfacial abdominal wall block technique will provide superior pain relief and reduce opioid requirements during recovery.

Eligibility Criteria

Inclusion Criteria: * Scheduled for elective gynecological video-laparoscopic surgery. * ASA physical status І-ІІ. * Age between 18 and 65 years. * Patient's informed consent to participate in the study Exclusion Criteria: * Known allergy or contraindications to local anesthetics. * Infection at the potential needle insertion sites. * Coagulopathy or ongoing anticoagulant therapy. * Conversion to open laparotomy during surgery. * Severe cognitive impairment or psychiatric disorders.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07705516). StuddyBuddy aggregates publicly available trial information.