Investigating the outcome and side effects of intrathecal morphine injection in posterior fusion surgery of patients with idiopathic scoliosis

Phase 3

Recruiting

• Conditions: Outcome and complications of intrathecal morphine injection in posterior fusion surgery of patients with idiopathic scoliosis.; M41.0; Infantile idiopathic scoliosis

• Registration Number: IRCT20240217061034N1
• Lead Sponsor: Oroumia University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 27 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Patients in need of posterior fusion surgery, patients with idiopathic scoliosis referred to Imam Khomeini Hospital , 10 to 20 years old
with physical status I, II, American Society of Anesthesiologists (ASA)
Children with idiopathic scoliosis in the range of 10 to 20 years

Exclusion Criteria

Symptoms of L2-3
intervertebral nerve injury Known allergy to one or more drugs used in the study
protocol History of corticosteroid use Opium and NSAIDs
in at least one week Coagulation dysfunction,
infection at the puncture site Cognitive impairment (inability to understand VAS)
Body mass index (BMI) greater than 35 kg/m2

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain intensity based on the pain felt by the patient. Timepoint: In recovery, it will be evaluated 0 to 2, 2 to 6, 6 to 12, and 12 to 24 hours after the operation. Method of measurement: pain scale (VAS).;Nausea/vomiting/itching. Timepoint: In recovery, it will be evaluated 0 to 2, 2 to 6, 6 to 12, and 12 to 24 hours after the operation. Method of measurement: Physical examination.;The first time to ask for painkillers. Timepoint: 24 hours after the operation. Method of measurement: Painkiller request by the patient.