Tokyo, Aug. 27 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000062704) titled 'The significance of lipid change analysis in scoliosis surgery' on Aug. 26.
Study Type:
Observational
Primary Sponsor:
Institute - The University of Tokyo
Condition:
Condition - Scoliosis
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - This study aims to investigate the perioperative dynamics of lipid mediators in posterior spinal fusion for scoliosis, a procedure associated with significant surgical invasiveness and severe postoperative pain. Posterior spinal fusion involves placing pedicle screws into the vertebrae and connecting them with rods to correct spinal curvature. Because of its invasiveness, postoperative pain management is often challenging. By examining temporal changes in lipid mediators during the perioperative period, we seek to identify novel therapeutic targets for inflammation and postoperative pain. Such approaches may reduce complications through improved inflammation control, facilitate earlier mobilization and discharge by alleviating postoperative pain, and ultimately contribute to better patient outcomes.
Basic objectives2 - Others
Eligibility:
Age-lower limit - 10
years-old
=
Gender - Male and Female
Key inclusion criteria - Patients diagnosed with scoliosis and scheduled to undergo posterior spinal fusion under general anesthesia at the University of Tokyo Hospital
Patients aged 10 years or older and 20 years or younger
Patients who understand the purpose of this study and provide informed consent
Key exclusion criteria - Patients for whom surgical cooperation cannot be obtained
Patients taking NSAIDs or tramadol preoperatively
Patients using prostaglandin preparations or lipid mediator antagonists (e.g., montelukast) preoperatively
Patients undergoing reoperation
Patients requiring chronic respiratory support due to scoliosis curvature
Target Size - 15
Recruitment Status:
Recruitment status - No longer recruiting
Date of protocol fixation - 2025 Year 12 Month 04 Day
Date of IRB - 2025 Year 10 Month 04 Day
Anticipated trial start date - 2025 Year 12 Month 08 Day
Last follow-up date - 2030 Year 03 Month 01 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067731
Disclaimer: Curated by HT Syndication.