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ENROLLING BY INVITATION
NCT06067893
PHASE4

Low Dose Dexmedetomidine as a Postoperative Pain Adjunct

Sponsor: Nichole Doyle

View on ClinicalTrials.gov

Summary

This randomized controlled trial examines whether the addition of a low-dose dexmedetomidine infusion to our current multimodal pain management plan decreases narcotic consumption and reduces side effects in adolescent patients undergoing posterior spinal fusion for idiopathic scoliosis.

Official title: Dexmedetomidine as a Pain Management Adjunct in the Pediatric Population Undergoing Posterior Spinal Fusion

Key Details

Gender

All

Age Range

10 Years - 21 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2024-07-01

Completion Date

2026-07

Last Updated

2025-12-22

Healthy Volunteers

Yes

Interventions

DRUG

Dexmedetomidine

Patient receives dexmedetomidine for 48 hours post-operatively

DRUG

Normal Saline

Patient receives normal saline for 48 hours post-operatively

Locations (1)

Children's Mercy Hospital

Kansas City, Missouri, United States