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Human study for investigating the effectiveness and safety of Cynanchum wilfordii on control of blood cholesterol

Human study for investigating the effectiveness and safety of Cynanchum wilfordii on control of blood cholesterol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0001733
Enrollment
84
Registered
2015-12-15
Start date
2015-12-02
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 : Subjects were randomly allocated to placebo group or Cynanchum wilfordii extract group (low dose or high dose). Then subjects consume palcebo or Cynanchum wilfordii extract once a

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Subject who voluntarily agrees to participate and sign in informed consent form 2) Adults (20 years = Age, both male and female) 3) 18 kg/m2 = BMI (Body Mass Index) = 30 kg/m2 4) Fasting blood LDL-cholesterol level = 130 mg/dL 5) Fasting blood triglyceride level< 300 mg/dL

Exclusion criteria

Exclusion criteria: 1) Fasting blood LDL-cholesterol level = 190mg/dL 2) Subjects who had consistently consumed the drug related to lipid metabolism (ex. statin, diuretics, beta blocker.. etc.) or inflammation metabolism within 4 weeks before the first visit. The subject who have taken thiazide and beta blockers among the diuretics without change of dose during last one year and expected not to change the dosage during the study period. 3) Subjects who consumed the functional food or food related to lipid metabolism or inflammation within 4 weeks before the first visit (example: plantsterol, w-3 fatty acid, aloe, chitosan, onion extract. etc.) 4) Subjects who are controlling body weight or subjects who have changed of body weight more than 10&#37; within 6 month before the first visit 5) Following diseases : - myocardial infarction, stroke - hypertension (Systolic Blood Pressure =140 mmHg OR Diastolic Blood Pressure =100 mmHg) - Diabetes (fasting glucose level = 180 mg/dL) - Liver dysfunction (AST, ALT = 2.5 X upper limit of normal range) - Renal dysfunction (serum creatinine = 1.4 mg/dL) - Chronic inflammatory bowel disease - Autoimmune disease, hyperthyroidism, hypothyroidism or malignant tumor 6) Women receiving hormone therapy 7) Chronic smoker (= 20 cigarettes / day) 8) Subjects with alcoholism or subjects who consume of alcohol more than 140g per week (example: soju about 2.5 bottles/week OR 2.5 glasses/day) 9) Excessive exercise (= 10 hours / week) 10) Participation in other human study within 4 weeks before the first visit 11) Subjects who are sensitive to Cynanchum wilfordii 12) Pregnant or lactating women 13) Any condition that the principal investigator believes may put the subjects at undue risk

Design outcomes

Primary

MeasureTime frame
Blood lipid profiles

Secondary

MeasureTime frame
Markers of inflammation and blood circulation ;Vital sign, adverse events;Clinical pathology examination, electrocardiography

Countries

Korea, Republic of

Contacts

Public ContactYoung Hong

Seoul National University Hospital

lottie0@hanmail.net+82-2-2072-3336

Outcome results

None listed

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