Spinal Fusion Clinical Trials

Clinical trials related to Spinal Fusion Procedure

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

Status: Recruiting
Location: See location...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to compare the analgesic efficacy of multiple mid-transverse process to pleura (MTP) block and PCA in idiopathic scoliosis patients undergoing posterior spinal fusion surgery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years.

• Both sexes.

• American Society of Anesthesiology (ASA) physical status I-II.

• Idiopathic scoliosis patients undergoing posterior spinal fusion surgery.

Locations
Other Locations
Egypt
Tanta University
RECRUITING
Tanta
Contact Information
Primary
Mohammed S Elsharkawy, MD
mselsharkawy@med.tanta.edu.eg
00201148207870
Time Frame
Start Date: 2025-02-12
Estimated Completion Date: 2026-12-01
Participants
Target number of participants: 40
Treatments
Experimental: MTP group
Patients will receive multiple mid-transverse process to pleura (MTP) block after induction of anesthesia.
Experimental: PCA group
Patients will receive IV-PCA. Morphine is generally administered as an initial loading dose of 0.05-0.1 mg/kg before the end of surgery, with PCA settings of a bolus dose of 0.01-0.03 mg/kg, a lockout interval of 6-10 min, and a background infusion of 0.01-0.02 mg/kg/h.
Related Therapeutic Areas
Sponsors
Leads: Tanta University

This content was sourced from clinicaltrials.gov