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Examination about the pharmacokinetics of the dexamethasone under the Fosaprepitant medication to the nausea and vomiting of an high emetic risk chemotherapy.

Not Applicable
Conditions
Inoperable advanced/recurrence Gastric Cancer or Esophageal Cancer or Colorectal Cancer
Registration Number
JPRN-UMIN000013782
Lead Sponsor
Osaka Medical College Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
12
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Patient who is taking Pimozide. (2) Patient who has severe liver failure or renal failure. (3) Patient who had been treated with one moderate risk emetogenic antitumour drug according to the 2014 National Comprehensive Cancer Network Clinical Practice Guidelines. (4) Patient who has vomited or provoked nausea in the 24 hours prior to start of chemotherapy. (5) Patient who is considered inappropriate as a target patient by a physician-in-charge.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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