Overview

Continuous Infusion Versus Intermittent Bolus Injection of Rocuronium

Status:
Unknown status
Trial end date:
2018-03-01
Target enrollment:
0
Participant gender:
All
Summary
The research is to find out whether continuous infusion of rocuronium requires more or less amount of rocuronium, per kilogram and per hour, than bolus administered rocuronium during noncardiac surgery.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Seoul National University Hospital
Treatments:
Bromides
Rocuronium
Criteria
Inclusion Criteria:

- Pediatric patients aged between 2 and 12, undergoing elective noncardiac surgery which
requires general anesthesia but does not require intense block, and estimated time of
surgery is between 2 and 5 hours

Exclusion Criteria:

- ASA class 3-6

- BMI >= 30

- Previous history of hepatic failure, renal failure or neuromuscular disease

- Patients taking medicine which interacts with rocuronium bromide, before or during
surgery: aminoglycosides, lincosamides, acylamino-penicillin antibiotics,
tetracyclines, metronidazole (high dose), diuretics, MAO inhibitors, calcium channel
blockers, corticosteroids, phenytoin, carbamazepine, or norepinephrine

- Previous history of allergic reaction (including anaphylactic reaction) and/or
malignant hyperthermia during general anesthesia

- Patients taking medicines which contains magnesium