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Verification of herbal treatment effect on diabetic and impaired glucose tolerance

Analysis of characteristics of diabetic and impaired glucose tolerance patients and evaluation of herbal treatment effectiveness

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0003793
Enrollment
100
Registered
2019-04-16
Start date
2018-05-15
Completion date
Unknown
Last updated
2019-04-23

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

Conditions

None listed

Interventions

None listed

Sponsors

Semyung University Oriental Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Those who are between 20 and 80 years of age 2. Diabetic patients taking or administering an oral hypoglycemic agent or insulin OR Those with a fasting blood glucose level of 110 mg / dL or more OR those with a blood glucose level of 140 mg / dL or more for 2 hours after a meal 3. A person who voluntarily signs a clinical study agreement 4. Those who are willing to cooperate during the study period and who will comply with the restrictions

Exclusion criteria

Exclusion criteria: 1. Subjects with a history of drug hypersensitivity to medicines and food ingredients 2. Subjects who have severe cerebrovascular disease (cerebral infarction, cerebral hemorrhage, etc.), heart disease (angina pectoris, myocardial infarction, heart failure, arrhythmia requiring treatment), pulmonary disease (chronic obstructive pulmonary disease, etc.) within the last 6 months (However, patients who have a history of cerebrovascular disease or heart disease but are clinically stable can participate in the test by the judgment of the tester.) 3. Severe dysfunction of liver and kidney (ALT, AST = 2.5 times the upper limit of normal) (Creatinine> 2.0 mg / dl) 4. Diagnosis of malignancy within 3 years before screening 5. In the opinion of the person in charge of testing applied to the human body, the person who is judged to be unable to comply with the test 6. People with mental illness who are difficult to communicate 7. Subject of pregnancy

Design outcomes

Primary

MeasureTime frame
Improvement of blood glucose;Change of HbA1C;Change of HbA1C-IFCC1;Change of HbA1C-IFCC2

Secondary

MeasureTime frame
body fat percentage;liver function test;lipid test;kidney function test

Countries

Korea, Republic of

Contacts

Public ContactSeon-mi Shin

Semyung University

bunggujy21@hanmail.net+82-43-649-1873

Outcome results

None listed

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