Comparing pain relief methods for scoliosis surgery patients

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• Tanta University
  Tanta, El-Gharbia, Egypt Recruiting

Study contacts

• Study coordinator: Mohammed S Elsharkawy, MD
• Email: mselsharkawy@med.tanta.edu.eg
• Phone: 00201148207870

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.