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Clinical Trial Summary

Oral olanzapine showed superior antiemetic efficacy to metoclopramide as rescue treatment to control breakthrough emesis induced by chemotherapy. This study aims to evaluate safety and efficacy of olanzapine for nausea and vomiting in advanced cancer patients.


Clinical Trial Description

This will be a pilot study; open-label prospective clinical trial. Oral olanzapine 5 mg tablet will be given to patients who fail two standard treatment medications for nausea and vomiting within 30 minutes after the first vomiting episode. Other doses of olanzapine will be given at 12, 24, and 36 hours following the first dose concurrently with standard regimen.

Patients with emesis will be followed up after receiving olanzapine every 12 hour for 48 hours. We will record the frequency of vomiting, nausea, and retching. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03679182
Study type Interventional
Source Khon Kaen University
Contact Jarin Chindaprasirt, MD
Phone +66846831097
Email jarich@kku.ac.th
Status Recruiting
Phase Phase 2
Start date September 1, 2018
Completion date September 2021

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