Comparing two pain relief techniques for lower abdominal surgery
Comparison Between the Analgesic Effects of Ultrasound-guided Unilateral Quadratus Lumborum Block (lateral Approach) Versus Erector Spinae Plane Block in Patients Undergoing Unilateral Lower Abdominal Surgery
This study is testing which pain relief method works better for adults having lower abdominal surgery: the Quadratus Lumborum Block or the Erector Spinae Plane Block.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 48 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Fayoum University Hospital Academic / other |
| Locations | 1 site (Al Fayyūm, Fayoum Governorate) |
| Trial ID | NCT05524038 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the analgesic effects of the Quadratus Lumborum Block and the Erector Spinae Plane Block in adults undergoing lower abdominal surgeries. Conducted at Fayoum University Hospital, the trial involves preoperative assessments, randomization, and the use of ultrasound-guided techniques for administering local anesthetics. Participants will be monitored throughout the procedure to evaluate pain relief and overall effectiveness of the interventions. The study is designed to provide insights into which technique offers better pain management for patients.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-60 scheduled for elective abdominal surgeries with ASA classification I or II.
Not a fit: Patients with coagulation disorders, skin infections at the injection site, or those with a known allergy to local anesthetics may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing lower abdominal surgeries.
How similar studies have performed: Other studies have shown promising results with similar analgesic techniques, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients age 18-60 years old. * Patients scheduled for elective abdominal surgeries * ASA classification I, II. * Ability to sign the consent. Exclusion Criteria: * Patient refusal. * Coagulation disorders. * Skin lesions or infection at site of proposed needle. * Known allergy to local anesthetics, or opioids. * Patients suffering from neurological or mental disease. * Opioid consumption 48 hours before the operation. * Sever Obesity body mass index(BMI) \>35 * Difficulty in Ultrasonographic identification.
Where this trial is running
Al Fayyūm, Fayoum Governorate
- Fayoum University hospital — Al Fayyūm, Fayoum Governorate, Egypt (Recruiting)
Study contacts
- Principal investigator: rana A. Abdelghaffar, MD — faculty of medicine ,Fayum university
- Study coordinator: mohamed M. abd elhamid elbarbary, master
- Email: mohamedelbarbary68@gmail.com
- Phone: o1o98756760
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.