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Optimal administration of fosaprepitant in patients with colon cancer

Phase 2
Conditions
Colon Cancer
Registration Number
JPRN-UMIN000010181
Lead Sponsor
Hitachi General Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients who previously developed serious or irreversible adverse effects at the administration site 2) Patients who were judged to be inappropriate as subjects by the study investigators

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain at the injection site evaluated by NRS
Secondary Outcome Measures
NameTimeMethod
Development site, time of development, duration of symptoms, reaction of injection site, and procedures to decrease symptoms
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