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The study of feasibility and usefulness of olanzapine for the patients who received oxaliplatin chemotherapy.

The study of feasibility and usefulness of olanzapine for the patients who received oxaliplatin chemotherapy. - The study of feasibility and usefulness of olanzapine for the patients who received oxaliplatin chemotherapy.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000032591
Enrollment
40
Registered
2018-05-15
Start date
2018-05-14
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

colorectal cancer

Interventions

Olanzapine
5mg PO on days 1 to 4 Aprepitant
125 mg PO on day 1, 80 mg PO on days 2 to 3 5HT3-receptor antagonist
IV administration on day 1 Dexamethasone
6.6 mg IV on day 1, 4 mg PO on days 2 to 3

Sponsors

Osaka International Cancer Institute
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Oxaliplatin-naive patients who receive the oxaliplatin (>=85mg/m2)-based chemotherapy 2. no limitation in TNM stage, recurrence, or metastatic unresectable. 3. no limitation of use of targeted therapy 4. Enough organ functions 5. Written informed consent

Exclusion criteria

Exclusion criteria: 1. Patients who has severe dysfunction of liver or kidney 2. Patients who suffered nausea or vomiting before 24 h of the enrollment 3. Patients who used antiemetics before 24 h of the enrollment 4. Patients with symptomatic brain metastasis/carcinomatosis. 5. Patients who had diabetes. 6. Pregnant, breastfeeding or expecting woman. 7. Patient is receiving pimozide 8. Patient is judged inappropriate by the investigator as subject for this study

Design outcomes

Primary

MeasureTime frame
The rate of adverse events

Countries

Japan

Contacts

Public ContactJunichi Nishimura

Osaka International Cancer Institute Department of Gastroenterological surgery

jnishimura@gesurg.med.osaka-u.ac.jp0669451181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026