Comparing pain relief methods after total abdominal hysterectomy
Ultrasound Guided Versus Surgical Rectus Sheath Block Versus Local Anesthesia Infiltration for Postoperative Analgesia in Patients Undergoing Total Abdominal Hysterectomy: A Randomized Trial
This study is testing three different ways to manage pain after a total abdominal hysterectomy to see which one works best for patients aged 18 to 65.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | Female |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06837532 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness and safety of three different methods for postoperative pain management in patients undergoing total abdominal hysterectomy: ultrasound-guided rectus sheath block, surgical rectus sheath block, and local anesthesia infiltration. The research will involve patients aged 18 to 65 who are scheduled for elective surgery and will assess pain relief outcomes and any associated complications. By comparing these techniques, the study seeks to identify the most effective approach for managing postoperative pain in this surgical population.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 65 scheduled for elective total abdominal hysterectomy with ASA physical status I or II.
Not a fit: Patients with hepatic, renal, or cardiac diseases, known allergies to local anesthetics, or those with chronic analgesic use 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 total abdominal hysterectomy.
How similar studies have performed: Previous studies have shown varying success with similar analgesic techniques, but this specific comparison is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age from 18 to 65 years old. * American Society of Anesthesiologists (ASA) physical status I - II. * Patients scheduled for elective total abdominal hysterectomy under general anesthesia. Exclusion Criteria: * Hepatic, renal or cardiac disease. * Any known allergy to local anesthetic. * Physical or mental conditions which may vaguely measure postoperative pain following surgery. * History of chronic use of analgesic as nonsteroidal anti-inflammatory drugs (NSAIDs) or central nervous system (CNS) depressants as antiepileptic, and bleeding disorders.
Where this trial is running
Cairo
- Ain Shams University — Cairo, Egypt (Recruiting)
Study contacts
- Study coordinator: Sarah A Afifi, MD
- Email: Sarah606060@gmail.com
- Phone: 0501035864
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.