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Comparison between Olanzapine- Aprepitant- Granisetron on nausea and vomiting

The comparison between Olanzapine- Aprepitant- Granisetron effects on chemotherapeutic drug induced nausea and vomiting in patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190217042735N1
Enrollment
105
Registered
2019-07-27
Start date
2019-07-09
Completion date
Unknown
Last updated
2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nausea and Vomiting. Nausea and vomiting

Interventions

Intervention 1: Intervention group: Olanzapine: 5mg Oral Olanzapine daily in 3 days. Intervention 2: Intervention group: Aprepitant: Kytril tablet 2mg+125mg oral Aprepitant on day one,80mg in second a

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Nausea and vomiting. Timepoint: First day and 48 to 72 hours after chemotherapy. Method of measurement: The patients will be monitored for nausea and vomiting on the first day and 48 to 72 hours after chemotherapy, and their clinical data will be recorded by the information form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarnoush Tajbakhsh

Zahedan University of Medical Sciences

f.tajbakhsh@zaums.ac.ir+98 54 3329 5744

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026