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Recruiting NCT06679569

NCT06679569 Deep Neuromuscular Blockade on Postoperative Pain

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Clinical Trial Summary
NCT ID NCT06679569
Status Recruiting
Phase
Sponsor Seoul National University Hospital
Condition Neuromuscular Blockade
Study Type INTERVENTIONAL
Enrollment 106 participants
Start Date 2024-11-06
Primary Completion 2026-11-06

Trial Parameters

Condition Neuromuscular Blockade
Sponsor Seoul National University Hospital
Study Type INTERVENTIONAL
Phase N/A
Enrollment 106
Sex ALL
Min Age 2 Months
Max Age 7 Years
Start Date 2024-11-06
Completion 2026-11-06
Interventions
rocuronium 0.2 mg/kg/hr continuous infusionrocuronium 0.6 mg/kg/hr continuous infusion

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Brief 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 Criteria

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.

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