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Search / Trial NCT07046949

Anterior Quadratus Lumborum Block as a Component of Multimodal Analgesia for Abdominal Hysterectomies

Launched by YURI SEMENYUK RIVNE REGIONAL CLINICAL HOSPITAL · Jun 23, 2025

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

Regional Anesthesia Quadratus Lumborum Block Abdominal Hysterectomy Pain Scores Multimodal Analgesia Acute Pain Chronic Pain Pain Management Opioid Consumption Quality Of Recovery Postoperative Nausea And Vomiting General Anesthesia Blended Anesthesia Hemodynamics After Surgery

ClinConnect Summary

This clinical trial is studying a new way to manage pain for women having abdominal hysterectomy surgery, which is the removal of the uterus often done for conditions like fibroids or other uterine problems. The researchers want to see if adding a special type of nerve block called an anterior quadratus lumborum (QL) block before surgery can help reduce the amount of opioid pain medication needed during and after the operation, lower pain levels, and improve overall recovery.

Women who are generally healthy (classified as ASA I or II) and have symptoms from fibroids or other uterine conditions, and are scheduled for an abdominal hysterectomy, may be eligible to take part. Participants will receive standard general anesthesia during surgery, and some will also get the QL nerve block while others will not, but neither the patients nor the doctors will know who gets the block during the study. This is to fairly test if the nerve block makes a difference. Important to note, women with very high body weight, uncontrolled high blood pressure, those already using certain opioid medications, or those who don’t want to participate will not be included. The trial is not yet recruiting, but if you qualify, you can expect careful monitoring of your pain and recovery after surgery to see if this nerve block helps improve your comfort and healing.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • patients with ASA status I-II
  • patients with symptomatic fibroids
  • patients scheduled for abdominl hysterectomy
  • Exclusion Criteria:
  • refusal to participate in the study at any of its stages
  • ASA class ≥ III
  • body mass index \> 40 kg/m2
  • use of opiate receptor agonists/antagonists before surgery
  • uncontrolled hypertension

About Yuri Semenyuk Rivne Regional Clinical Hospital

Yuri Semenyuk Rivne Regional Clinical Hospital is a leading healthcare institution committed to providing comprehensive medical services and advancing clinical research in the Rivne region. As a clinical trial sponsor, the hospital focuses on facilitating innovative studies aimed at improving patient outcomes and promoting evidence-based medical practices. With a multidisciplinary team of healthcare professionals and state-of-the-art facilities, the hospital plays a pivotal role in supporting clinical research initiatives that address regional health priorities and contribute to the broader medical community.

Locations

Rivne, Rivne Region, Ukraine

Patients applied

0 patients applied

Trial Officials

Olha Filyk, Professor

Study Chair

Danylo Halytsky Lviv National Medical University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported