Deep Neuromuscular Blockade on Postoperative Pain
ConditionNeuromuscular Blockade
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age2-7
SponsorSeoul National University Hospital
About this trial
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
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- rocuronium 0.2 mg/kg/hr continuous infusion
- rocuronium 0.6 mg/kg/hr continuous infusion
Treatment groups
106 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov