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Randomized Phase II trial of palonosetron, aprepitant plus dexamethasone for 1 day with or without dexamethasone on days 2 and 3 in the prevention of nausea and vomiting induced by chemotherapy for breast cancer

Phase 2
Conditions
breast cancer
Registration Number
JPRN-UMIN000006977
Lead Sponsor
Kitasato University School of Medicine Department of Surgery
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

1)Patients who has a convulsive disorders that need anticonvulsants therapy. 2)With nausea (CTCAE Grade2). 3)A history of sever allergic reaction with palonosetron or aprepitant or dexamethasone. 4)Pregnancy or the desire to preserve fecundity. 5)Receiving an antiemetic drug. 6)Receiving pimozide. 7)With mental disease or psychotic manifestation. 8)Any patients judged by the investigator to be unfit to participate in the study.

Study & Design

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