Phase
Condition
Lactose Intolerance
Colic
Stomach Discomfort
Treatment
OLA group: Olanzapine
DEX group: Dexamethasone
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
18 years and older
confirmed cancer diagnosis
starting cycle 1 of an FDA approved treatment that is categorized as high-emetogenic (nausea and vomiting inducing) chemotherapy per National Comprehensive CancerNetwork® guidelines
Eastern Cooperative Oncology Group performance score of 0 or 1
appropriate renal function
appropriate hepatic function
appropriate hematologic function.
Exclusion
Exclusion Criteria:
Patients will be excluded if they experience nausea or vomiting up to 24 hoursbefore chemotherapy,
currently on a glucocorticoid therapy
contraindication to glucocorticoid therapy
taking any medication that has antiemetic properties.
scheduled or planned to receive radiation within one week of or concurrently withchemotherapy
brain metastases.
Study Design
Study Description
Connect with a study center
Robert Packer Hospital
Sayre, Pennsylvania 18840
United StatesActive - Recruiting
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