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Clinical Trials/NCT00124930
NCT00124930
Terminated
Phase 3

A Randomized Double-blind, Parallel Group Study Comparing Olanzapine (Zyprexa) With Haloperidol (Novo-peridol) for the Relief of Nausea and Vomiting in Patients With Advanced Cancer

Alberta Health services1 site in 1 country80 target enrollmentMay 2005

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Nausea
Sponsor
Alberta Health services
Enrollment
80
Locations
1
Primary Endpoint
Severity of nausea on days 3 and 5
Status
Terminated
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to compare the efficacy and safety of Haldol (haloperidol) and olanzapine in the control of chronic nausea with advanced cancer patients who have failed first line antiemetic therapy.

Detailed Description

The purpose of this study is to compare the efficacy and safety of haloperidol and olanzapine in the control of chronic nausea with advanced cancer patients who have failed first line antiemetic therapy.

Registry
clinicaltrials.gov
Start Date
May 2005
End Date
June 2008
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • \>18 years of age
  • Significant nausea/vomiting
  • Failed maxeran and domperidone
  • Underlying treatment of causes has failed
  • Adequate cognitive function
  • Communicates well

Exclusion Criteria

  • Partial/complete bowel obstruction
  • Currently taking Haldol or olanzapine
  • Has drug induced extrapyramidal symptoms
  • Parkinson's disease
  • Undergoing chemotherapy or radiotherapy (RT) to brain, abdomen, stomach or esophagus

Outcomes

Primary Outcomes

Severity of nausea on days 3 and 5

Study Sites (1)

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