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Efficacy and Safety of Chrysanthemum indicum extract on reducing body weight and body fat of overweight subjects

Efficacy and Safety of Chrysanthemum indicum extract on reducing body weight and body fat of overweight subjects; A 12 week, Randomized, Double-blind, Placebo-Controlled Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002492
Enrollment
100
Registered
2017-10-12
Start date
2017-05-23
Completion date
Unknown
Last updated
2019-03-11

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 : Take 2 capsules once a day for 12 weeks with randomly assigned doses of 452 mg / capsule (hamcho extract 250 mg / capsule) or control group (Placebo).

Sponsors

Wonkwang Pharmaceutical
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) A person who agrees to participate in this study and who voluntarily signs the written agreement (2) Adult men and women aged 20 years or older and younger than 60 years (3) Those with a BMI of at least 25 kg / m2 and less than 30 kg / m2.

Exclusion criteria

Exclusion criteria: (1) Subjects with severe cerebrovascular disease (cerebral infarction, cerebral hemorrhage, etc.), heart disease (angina pectoris, myocardial infarction, heart failure, arrhythmia requiring treatment) within the past 6 months If the test subject has a history but is clinically stable, he / she can participate in the test by the testee's judgment.) (2) patients with uncontrolled hypertension (blood pressure of 160/100 mmHg or higher, after 10 minutes of test subjects) (3) Diabetic patients taking fasting blood glucose levels greater than 126 mg / dl, randomized blood glucose levels greater than 200 mg / dl, or taking oral hypoglycemic agents or insulin (4) TSH not more than 0.1 uU / ml or not less than 10 uU / ml (5) Creatinine Those who are more than twice the normal upper limit of the test institute (6) AST (GOT) or ALT (GPT) A person who is at least three times the normal upper limit of the testing laboratory (7) Those who complain of severe gastrointestinal symptoms such as heartburn, indigestion, etc. (8) Drugs that affect weight within the past month (including absorption inhibitors and appetite suppressants, health functional foods / supplements related to obesity improvement, psychiatric drugs such as depression, beta blockers, diuretics, birth control pills, steroids, A person taking (9) Those who participated in the commercial obesity program within the last 3 months (10) Have participated or planned to participate in other clinical trials within the past one month (11) Alcohol use through medical history, etc. ? Those who are admitted to hospital, medication or rehabilitation due to induced disorder, heart disease, central nervous disorder (12) Those who are judged to be unable to exercise due to musculoskeletal disorders (13) Anyone who is pregnant or has a pregnancy plan for the duration of the test (14) Any person who is found to be inadequate by the tester for other reasons

Design outcomes

Primary

MeasureTime frame
Body fat percentage through DEXA

Secondary

MeasureTime frame
Weight;Waist circumference, hip circumference, waist / hip circumference ratio;Fat mass through DEXA;Fat mass through DEXA;CT visceral fat area, subcutaneous fat area, total abdominal fat area, visceral / subcutaneous fat area ratio;Lipid panel : Total Cholesterol, HDL-Cholesterol, LDL-Cholesterol, Triglyceride;hs-CRP, Adiponectin, Leptin

Countries

Korea, Republic of

Contacts

Public ContactKANG HEON

Inje University Seoul Paik Hospital

fmleader@nuri.net+82-2-2270-0907

Outcome results

None listed

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