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A study of the effectiveness of prophylactic granulocyte colony-stimulating factor (G-CSF) for patients with esophageal cancer who receive DCF therapy.

Phase 2
Conditions
esophageal cancer
Registration Number
JPRN-UMIN000015561
Lead Sponsor
Osaka University School of Medicine Gastroenterological Surgery
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
23
Inclusion Criteria

Not provided

Exclusion Criteria

1.G-CSF hypersensitivity. 2.Administration of G-CSF within 6 weeks. 3.Infection within 2 weeks. 4.Past history of chemotherapy or radiation therapy. 5.Patients who are pregnant, lactating, with child-bearing potential. 6.Patients who is judged by the investigator to be inappropriate for study participation for any reason.

Study & Design

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