Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06679569

Deep Neuromuscular Blockade on Postoperative Pain

Effect of Deep Neuromuscular Blockade on Postoperative Pain in Pediatric Patients Undergoing Laparoscopic Surgery: a Prospective Randomized Controlled Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
106 (estimated)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
2 Months – 7 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGrocuronium 0.2 mg/kg/hr continuous infusionTo 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.
DRUGrocuronium 0.6 mg/kg/hr continuous infusionTo 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.

Timeline

Start date
2024-11-06
Primary completion
2026-11-06
Completion
2026-11-07
First posted
2024-11-07
Last updated
2025-05-13

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06679569. Inclusion in this directory is not an endorsement.