Deep Neuromuscular Blockade on Postoperative Pain
Condition(s) studied
Investigational drug(s) / intervention(s)
rocuronium 0.2 mg/kg/hr continuous infusion: To maintain Train-of-four count 1 to 3 during surgery: Administration of continuous infusion of rocuronium at a rate of 0.2 mg/kg/hr to achieve and sustain moderate neuromuscular blockade.
rocuronium 0.6 mg/kg/hr continuous infusion: To maintain Train-of-four count 0 during surgery: Administration of continuous infusion of rocuronium at a rate of 0.6 mg/kg/hr to achieve and sustain deep neuromuscular blockade.
Study summary
This study aims to investigate the impact of varying degrees of neuromuscular blockade on postoperative pain in pediatric patients aged over 2 months to under 7 years undergoing laparoscopic surgery under general anesthesia.
Eligibility
Primary outcome measure(s)
- ANIm (Analgesia Nociception Index) Value — 30 minutes after arrival in the recovery room
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| SNUCH | Seoul | Seoul | Recruiting |
More Seoul National University Hospital trials in South Korea
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06679569 on ClinicalTrials.gov ↗ ← All trials in South Korea