None listed
Conditions
Interventions
Drug : GOK and placebo preparation sealed 120-mL packet of liquid GOK (GOK group) or liquid placebo (control group) twice a day after breakfast and dinner, for 4 weeks.
Sponsors
Catholic Kwandong University International St.Mary's Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: . Subjects were physically and mentally healthy males and females aged 21 to 60 who had seen one of the clinical trial flyers posted in the hospital between March and April 2015 and had willfully consented to participate
Exclusion criteria
Exclusion criteria: 1) underlying diseases including hypertension, hepatitis, or tuberculosis; 2) a history of endocrin ologic or hormone disorders; 3) a history of hepato-pancreato-biliary or renal disorders; 4) a history of impaired blood glucose regulation (i.e., impaired fasting glucose, impaired glucose tolerance, or diabetes); 5) steroid or hormonal drug use less than 1 month before the start of the study; 6) pregnancy or breastfeeding; and 7) any abnormal findings that might possibly have impacted the study results. The researchers first confirmed any matters that contravened the clinical trial conditions via a phone call or visit to each subject.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| fatigue severity scale short form health survey-36 | — |
Secondary
| Measure | Time frame |
|---|---|
| hematologic and serological | — |
Countries
Korea, Republic of
Contacts
Public Contactnarae yang
Catholic Kwandong University International St.Mary's Hospital
Outcome results
None listed