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
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.
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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