Trial intelligence / Profile preview

Intrathecal Ketamine and Morphine for Postoperative Pain in Abdominal Cancer Surgery

NCT02726828Phase 3

Key facts

Status
Completed
Start
Oct 2015
Primary completion
Feb 2016
Sponsor
Assiut University
Modality
Small Molecules
Conditions
postoperative pain
01

Overview

Phase 3, randomised, double-blind trial of ketamine in postoperative pain (3 arms), sponsored by Assiut University. Primary endpoints: Visual Analogue Scale, Time to first analgesic request and 1 more. Started Oct 2015; status: completed.

02

Design

3 arms
Study design
RandomizedDouble-blind
  • Morphine Group

    Morphine 0.3mg + Bupivacaine

  • Ketamine Group

    Ketamine 0.1mg/kg + Bupivacaine

  • Combination Group

    Morphine 0.3mg + Ketamine 0.1mg/kg + Bupivacaine

03

Who it enrols

Adult patients aged 30-50 undergoing major abdominal cancer surgery, excluding those with significant organ disease, coagulation disorders, or BMI > 30.

04

Endpoints

Primary

  • Visual Analogue Scale

  • Time to first analgesic request

  • Total analgesic consumption

Secondary

  • Side effects

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