drugset / Trial / NCT01236495

Comparison for Pethidine Requirement in Patients Received Spinal Morphine 0.2 and 0.3 mg for Post Lobectomy Analgesia

NCT01236495 ↗

Phase 4 Completed 40 enrolled Mahidol University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate the amount of total pethidine requirement during the 48 hour postoperative period after receiving spinal morphine 0.2 and 0.3 mg.

Timeline

Start
2010-11
Primary completion
2012-03
Completion
2012-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Morphine Other / unclassified 0.2 mg Other
Comparator Morphine Other / unclassified 0.3 mg Other

Indications