drugset / Trial / NCT06946277

Assessing the Time-Course of Dexmedetomidine-Induced Analgesia Via EEG

NCT06946277 ↗

Phase 4 Not yet recruiting 20 enrolled China International Neuroscience Institution
NaSingle-groupOpen-labelHealth-services research

Summary

Objective: To investigate the temporal dynamics of dexmedetomidine's analgesic effects in the brain using EEG. Methods: Eligible patients scheduled for total hip arthroplasty under intrathecal anesthesia received a continuous infusion of DEX at 1.5 μg/(kg·h) for 15 minutes before neuraxial puncture, followed by an additional 15-minute infusion. The study was divided into three phases: Phase 1: Non-dosing phase (Baseline). Phase 2: DEX preemptive analgesia phase (DEX infusion). Phase 3: DEX cessation phase (Post-infusion). Outcomes: Primary safety outcome: EEG spectral analysis at different phases. Secondary outcomes: NRS scores, postoperative nausea and vomiting (PONV), dizziness, agitation, and time to intestinal exhaust within 48 hours. Intraoperative hemodynamics were also monitored.

Timeline

Start
2025-04-25
Primary completion
2025-05-25
Completion
2025-05-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexmedetomidine Other / unclassified 1.5 ug/kg —

Indications