Comparing pain relief methods for scoliosis surgery patients
Comparison of Analgesic Efficacy of Multiple Mid-Transverse Process to Pleura (MTP) Block and PCA in Idiopathic Scoliosis Patients Undergoing Posterior Spinal Fusion: A Randomized Clinical Trial
This study tests whether a new pain relief method works better than the standard one for patients recovering from scoliosis surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Tanta University Academic / other |
| Locations | 1 site (Tanta, El-Gharbia) |
| Trial ID | NCT06820190 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of multiple mid-transverse process to pleura (MTP) block versus patient-controlled analgesia (PCA) for managing postoperative pain in patients with idiopathic scoliosis undergoing posterior spinal fusion surgery. The research focuses on improving pain management strategies to enhance recovery and reduce hospitalization time. By utilizing advanced regional anesthesia techniques, the study aims to provide insights into optimal pain control methods for this specific patient population.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with idiopathic scoliosis scheduled for posterior spinal fusion surgery.
Not a fit: Patients with pre-existing infections, allergies to study drugs, or significant comorbidities may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for scoliosis surgery patients, enhancing their recovery experience.
How similar studies have performed: Other studies have shown promise with regional anesthesia techniques like MTP blocks, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥ 18 years. * Both sexes. * American Society of Anesthesiology (ASA) physical status I-II. * Idiopathic scoliosis patients undergoing posterior spinal fusion surgery. Exclusion Criteria: * Patients with pre-existing infection at block site. * Known allergy to study drugs. * Coagulation disorder. * History of psychiatric illness. * Pre-existing neurological deficits. * Patient with morbid obesity (body mass index \>40 kg/m2). * Presence of any pre-operative pain or history of chronic pain. * History of regular analgesic.
Where this trial is running
Tanta, El-Gharbia
- Tanta University — Tanta, El-Gharbia, Egypt (Recruiting)
Study contacts
- Study coordinator: Mohammed S Elsharkawy, MD
- Email: mselsharkawy@med.tanta.edu.eg
- Phone: 00201148207870
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.