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A study on the prevention of exacerbation of oral mucositis by early initiation of Episil oral liquid in hematopoietic stem cell transplant recipients and head and neck cancer patients

Not Applicable
Recruiting
Conditions
Head and neck cancer, Hematological malignancy
Registration Number
JPRN-UMIN000045409
Lead Sponsor
Fujita Health University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
90
Inclusion Criteria

Not provided

Exclusion Criteria

1) Patients who need assistance in using Episil. 2) Patients with lesions including the central nervous system (CNS), or having confirmed/suspected of metastasis/invasion in the CNS 3) Patients using opioids for pain management prior to the start of Episil administration. 4) Patients with serious infections or complication. 5) Patients with known allergy to any of the ingredients in Episil. 6) Patients judged to be inappropriate by the investigator.

Study & Design

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

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