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Palonosetron+Aprepitant+Dexamethasone for moderately emetic chemotherapy induced nausea and voimiting-Phase II study

Phase 2
Completed
Conditions
ung cancer
Registration Number
JPRN-UMIN000004936
Lead Sponsor
iigata Lung Cancer Treatment Group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
160
Inclusion Criteria

Not provided

Exclusion Criteria

1)MEC administration except Day 1. 2)Radiation therapy 3)Contraindication of Dexamethasone 4)Symptomatic brain meta 5)Hypersensitivity for Palonosetron, Aprepitant, Dexamethasone 6)Vomiting episode prior to chemotherapy with 24 hours

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete response rate in 1st course of chemotherapy
Secondary Outcome Measures
NameTimeMethod
Complete response rate in any course of chemotherapy Complete control rate Time to treatment failure QOL analysis Toxicity
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