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The efficacy and safety of antiemetic therapy for carboplatin-containing chemotherapy-induced nausea and vomiting in patients with lung cancer.

Phase 2
Conditions
advanced lung cancer
Registration Number
JPRN-UMIN000026739
Lead Sponsor
Second Division, Department of Internal Medicine, Hamamatsu university school of medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

1)patients with the history of hypersensitivity or allergy for study drugs. 2)patients who need and use antiemetic therapy during 48h before chemotherapy. 3)patients with severe hepatic or renal dysfunction. 4)With convulsion. 5)Patients who need puncture to manage ascites. 6)Patients with complications inducing nausea and vomiting. 7)Patients with diabetes mellitus. 8)Patients who are judged to be inappropriate for this study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete response rate during the 120 h after carboplatin administration.
Secondary Outcome Measures
NameTimeMethod
Complete response rate during the acute, delayed phase. Complete control rate, safety.
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