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A verification study of the alleviation effects on symptoms after recovery from COVID-19 by using AHCC (R) with activity of enhancing human immune function including anti-virus immunity

Not Applicable
Conditions
Healthy Japanese subjects
Registration Number
JPRN-UMIN000049766
Lead Sponsor
ORTHOMEDICO Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
44
Inclusion Criteria

Not provided

Exclusion Criteria

1. Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3. Subjects currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4. Subjects who suffered from diseases (e.g., lifestyle disease, cardiac diseases, cancer, or respiratory diseases) except for post-COVID-19 symptoms after recovery from COVID-19 5. Subjects who have been diagnosed with post-COVID-19 symptoms 6. Subjects who use or take "Foods for Specified Health Uses," or "Foods with Functional Claims" in daily 7. Subjects who are currently taking medications (including herbal medicines) and supplements 8. Subjects who are allergic to medicines and/or the test food related products 9. Subjects who are pregnant, lactating, or planning to become pregnant during this trial 10. Subjects who suffer from COVID-19 11. Subjects who have been enrolled in other clinical trials within the last 28 days before the agreement to participate in this trial or plan to participate another trial during this trial 12. Subjects who are judged as ineligible to participate in this study by the physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. The proportion of subjects whose "Degree of Symptoms (score)" decrease by one point or more in one or more of the corresponding "Major Symptoms" as listed in the consultation checklist for patients with post-COVID-19 symptoms
Secondary Outcome Measures
NameTimeMethod
1. The subjective symptoms questionnaires, saliva test
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