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Feasibility study of food containing Acanthopanax senticosus for cancer related fatigue

Not Applicable
Conditions
Cancer related fatigue (malaise)
Registration Number
JPRN-UMIN000043988
Lead Sponsor
Health Sciences University of Hokkaido
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
15
Inclusion Criteria

Not provided

Exclusion Criteria

#1 The patients who have taken Acanthopanax Senticosus and are not off it for more than 3 months. #2 Allergy to Acanthopanax Senticosus and/or chlorella and/or honey. #3 Breast, uterus and ovary cancer patient who are histologically confirmed with estrogen receptor positive. #4 The patient who received Doxifluridine (FURTULON) chemotherapy. #5 Uncontrolled hypertension (Blood pressure more than 180/90 mmHg) #6 Currently taking digoxin formulation. #7 Co-existence of severe complication. #8 Pregnant or expected to be pregnant, and breast feeding mother. #9 Co-existence of endometriosis and myoma uteri. #10 Unable to provide and written informed consent due to mental disorder. #11 Concomitant use of drugs which is contraindicated towards either Acanthopanax Senticosus or chlorella.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The proportion of the patient whose BFI can be evaluated at "visit 2".
Secondary Outcome Measures
NameTimeMethod
# The rate of improvement in cancer-related fatigue # The changes in laboratory data # Safety (The frequency of total adverse event)
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