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Recruiting Not applicable

Deep Neuromuscular Blockade on Postoperative Pain

NCT06679569 · tracked via the Priya Life Science South Korea tracker
Phase
Not applicable
Started
2024-11-06
Last updated
2025-05-13

Condition(s) studied

Neuromuscular Blockade

Investigational drug(s) / intervention(s)

rocuronium 0.2 mg/kg/hr continuous infusionrocuronium 0.6 mg/kg/hr continuous infusion

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

Sex
ALL
Min age
2 Months
Max age
7 Years
Healthy volunteers
No
Inclusion Criteria: * Pediatric patients aged over 2 months to under 7 years scheduled for laparoscopic surgery under general anesthesia. * American Society of Anesthesiologists (ASA) Physical Status Classification I, II, or III. Exclusion Criteria: * Patients undergoing emergency surgery. * Patients with chronic pain or currently taking analgesics for chronic pain. * Known hypersensitivity to general anesthetic agents or analgesics. * Patients with underlying cardiovascular disease. * Patients with neuromuscular disorders. * Any other condition that, in the investigator's judgment, would make the patient unsuitable for participation in the study.

Primary outcome measure(s)

  • ANIm (Analgesia Nociception Index) Value — 30 minutes after arrival in the recovery room

Trial sites (1)

FacilityCityRegionStatus
SNUCH Seoul Seoul Recruiting
Official registry record

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