drugset / Trial / NCT01546948

Intraoperative Opioids and Postoperative Recovery After Hepatobiliary or Foregut Surgery

NCT01546948

Phase 4 Completed 60 enrolled Endeavor Health
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary aim of this randomized, double-blind study is to examine the effect of a single intraoperative dose of methadone on analgesic requirements during the first three days after hepatobiliary or foregut surgery. These patients will be compared to subjects receiving a standard dose of the "traditional" intraoperative opioid (hydromorphone). Secondary outcome measures to be assessed will include postoperative pain scores and standard recovery variables such as hospital length of stay.

Timeline

Start
2011-08
Primary completion
2018-06
Completion
2018-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Hydromorphone Other / unclassified 0.03 mg/kg
Subject Methadone Other / unclassified 0.3 mg/kg

Indications

No indication recorded.