Propofol + Remifentanil vs. Propofol + Dexmedetomidine in Adolescent Idiopathic Scoliosis Patients Having Spine Surgery
Launched by CEDARS-SINAI MEDICAL CENTER · Oct 19, 2023
Trial Information
Current as of July 09, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying two different combinations of medications used for anesthesia during spine surgery in teenagers with Adolescent Idiopathic Scoliosis. The goal is to find out which combination provides better pain control after the surgery. Participants will be randomly chosen to receive either Propofol and Remifentanil, which is commonly used at our hospital, or Propofol and Dexmedetomidine, which is more often used in adult surgeries. The researchers believe that using Dexmedetomidine may help reduce the need for extra pain medication after surgery, leading to less pain sensitivity.
To participate, you need to be between 12 and 18 years old and diagnosed with Adolescent Idiopathic Scoliosis, and you must be having a specific type of surgery called posterior spinal fusion. The study is currently recruiting participants, and those who join can expect to be monitored closely for pain levels and recovery times after the surgery. The findings from this trial may help improve pain management strategies for children undergoing spine surgery in the future.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 12-18 years old
- • American Society of Anesthesiology Physical Status Classification (ASA Class) 1 and 2
- • Have diagnosis of Adolescent Idiopathic Scoliosis
- • Undergoing Posterior Spinal Fusion with instrumentation for scoliosis correction
- • Matched on age, sex, and the number of vertebral levels fused
- Exclusion Criteria:
- • Neuromuscular scoliosis
- • Allergy to any of the multi-modal analgesia regimen drugs
- • Use of serotonergic drugs, monoamine oxidase inhibitors (MAOI), mixed agonist/antagonist opioid analgesics
About Cedars Sinai Medical Center
Cedars-Sinai Medical Center is a renowned nonprofit academic medical center located in Los Angeles, California, recognized for its commitment to patient care, research, and education. As a leading institution in clinical trials, Cedars-Sinai harnesses innovative approaches to advance medical knowledge and improve treatment outcomes across various specialties. With a multidisciplinary team of experts, state-of-the-art facilities, and a patient-centered approach, Cedars-Sinai actively contributes to the development of novel therapies and interventions, ensuring the highest standards of clinical research while prioritizing patient safety and ethical considerations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Los Angeles, California, United States
Patients applied
Trial Officials
Glenn Tan, M.D.
Principal Investigator
Cedars-Sinai Medical Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported