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A clinical trial on the functionality and safety of C. lacerata mycelium cultures

A Double-blind, Randomized, Placebo-controlled Intervention Study of the Efficacy and Safety of “Submerged culture of Ceriporia Iacerata mycelium" in patients with impaired fasting glucose intolerance or mild type 2 diabetes subjects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007722
Enrollment
72
Registered
2022-09-21
Start date
2015-02-15
Completion date
Unknown
Last updated
2022-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Dietary Supplement : Ceriporia lacerata Tablets and Placebo Tablets - Ceriporia Lacerata Tablets Group: Take 2 tablets of Ceriporia lacerata (550 mg) 3 times a day on an empty stomach before each mea

Sponsors

Fugenbio
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Men between the ages of 20 and under 75 and non-lactating women with no possibility of pregnancy, except for the illiterate. 2. Subjects with a fasting blood sugar of 100 mg/dL or more and less than 140 mg/dL and HbA1c 7.0% or less, not taking diabetes medication 3. Subjects with a fasting blood sugar of less than 110 mg/dL or HbA1c 6.5% 7.0% 4. A person who voluntarily decides to participate and agrees in writing to abide by the precautions after hearing and fully understanding the detailed explanation of this human application test

Exclusion criteria

Exclusion criteria: 1. Subjects with adverse reactions such as allergies when taking medicines or health functional foods 2. Subjects with hypersensitivity to or a history of mushrooms 3. Gastrointestinal disorders that may affect the absorption of test products for human application (Example: Crohn's disease) or gastrointestinal surgery (however, simple appendectomy or Those with a history of hernia surgery) 4. Those who show the following results in a diagnostic medical test - AST, ALT > 2 times the upper limit of the normal range - Other significant diagnostic test findings 5. Those with the following clinically significant diseases Diabetics taking blood sugar lowering drugs or insulin, uncontrolled Hypertensive patients (140/90 or higher), blood LDL-cholesterol 160 or higher factor, thyroid dysfunction patients, depression, schizophrenia, alcoholism Patients with mental disorders such as heart disease, drug addiction, heart failure, angina pectoris, myocardial infarction, etc. Cardiovascular disease, acute and chronic liver disease (chronic type B, chronic type C) Hepatitis, various liver cirrhosis, liver cancer, etc.) 6. Obesity drugs, antidepressants, contraceptives, oral steroids within the last 1 month Lloyd, female hormones, thyroid hormones, etc. have been taken or tested Drugs that affect the absorption, metabolism, or excretion of food or to reduce blood sugar Subjects with experience taking drugs that may affect 7. Pregnant and lactating women 8. Those who participated in other human application tests within 1 month before the first intake date 9. In the opinion of the person in charge of testing for human application, it is necessary to follow the Subjects judged to be unsuitable or otherwise judged to be unsuitable by the physician.

Design outcomes

Primary

MeasureTime frame
Decrease in fasting blood sugar

Secondary

MeasureTime frame
changes in blood sugar after eating, changes in glycated hemoglobin (HbA1c) levels, changes in insulin levels, changes in C-peptide levels, changes in blood fat composition

Countries

Korea, Republic of

Contacts

Public ContactBo-Hyung Kim

Kyung Hee University Hospital

bhkim98@gmail.com+82-2-958-9579

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026