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Exploratory clinical study of silkworm cordyceps for targeting dementia patients

Phase 3
Recruiting
Conditions
Dementia
F00, F01, F02, F03
Registration Number
JPRN-jRCTs031200291
Lead Sponsor
Hiroyuki Osawa
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Dementia over the preceding 6 months as the following criteria
1.Persons with an MMSE result of 21 or less
2.Those who are not in the habit of taking foods containing Cordyceps
3.Those who do not regularly use supplements and health foods
4.Those who have no history of treatment for malignant tumor, heart failure, myocardial infarction
5.Those who are not allergic to foods and medicines containing Cordyceps
6.Those who fully understand the content of clinical trials and have written consent

Exclusion Criteria

1.Pregnant or breast-feeding woman or person who is willing to become pregnant during the test period
2.Those who are participating in other clinical trials and those who have participated in other clinical trials within 3 months
3.Those who cannot follow the instructions of the physicians and medical staff
4.A person who has been judged by a physicians to have any problems

Study & Design

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