drugset / Trial / NCT00540085

Pharmacodynamic Trial on Rocuronium in Obese Patients

NCT00540085

Phase 4 Completed 51 enrolled Rigshospitalet, Denmark
RandomizedParallel-groupTriple-blindPrevention

Summary

Aim: To optimize the use of rocuronium (a neuromuscular blocking agent) in obese patients undergoing gastric bypass or gastric banding. Background: During general anaesthesia, a neuromuscular blocking agent is needed to allow surgery and airway management. Optimal dosing is important in order to avoid inadequately muscle relaxation, but also to avoid overdosage, which can result in prolonged anaesthesia and respiratory complications. Main hypothesis: Rocuronium dosed according to ideal body weight results in shorter duration of action compared to rocuronium dosed according to corrected body weight without prolonged onset time or compromised airway management or surgical demands for muscle relaxation.

Timeline

Start
2007-10
Primary completion
2008-02
Completion
2008-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator Rocuronium Other / unclassified 0.6 mg/kg Intravenous

Indications

No indication recorded.