IRCT20190217042735N1RecruitingPhase 3
The comparison between Olanzapine- Aprepitant- Granisetron effects on chemotherapeutic drug induced nausea and vomiting in patients
Zahedan University of Medical Sciences0 sites105 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Sponsor
- Enrollment
- 105
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 65 years (—)
- Sex
- All
Inclusion Criteria
- •Informed consent
- •Receiving chemotherapy regimens with moderate and high nausea and vomiting
- •Serum Creatinine 2 or less
- •AST and ALT less than 3 times of normal upper limit
- •Absolute Neutrophil counts of more than 1500 cubic millimeters
- •Not having another cause for nausea and vomiting, such as brain tumors and stomach cancer
Exclusion Criteria
- •Having nausea and vomiting too much and uncontrollable
- •Having allergies or showing other side effects of medications
- •Pregnant and lactating women
- •Having chronic illnesses such as: severe heart failure, uncontrolled diabetes, cardiac arrhythmia and cardiac infarction over the past 6 months
- •Use of other interventions or confusing drugs (Quinolones, abdominal radiotherapy, other underlying conditions, etc.)
- •Treatment with other antipsychotic drugs (Risperidone, Quetiapine, Clozapine, Phenothiazine) 30 days before entering the study
- •Having known problem in the CNS (cerebral metastasis or seizure) or cognitive impairment
- •Having nausea and vomiting 24 hours before treatment
Investigators
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