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A human study to evaluate safety and effective dose of Phellinus baumii extract complex on platelet aggregation response and blood flow in healthy subjects given a dietary lipid challenge: a randomized, double-blind, placebo-controlled, cross-over study

A human study to evaluate safety and effective dose of Phellinus baumii extract complex on platelet aggregation response and blood flow in healthy subjects given a dietary lipid challenge: a randomized, double-blind, placebo-controlled, cross-over study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0001193
Enrollment
56
Registered
2014-08-05
Start date
2014-08-13
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 at placebo group, Phellinus baumii low group, Phellinus baumii intermediate group or Phellinus baumii high group. Then take with high fat liquid f

Sponsors

Ewha Womans University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subects who informed consent Healthy subjects (30-65 years)

Exclusion criteria

Exclusion criteria: BMI > 35kg/m2 body weight fluctuation of 10% or more in the past 8weeks excessive activity takes hormone therapy (female) excessive smoker drinking alcohol more than 140g/week platelet function disorder taking anti-platelet medication (aspirin, non-steroidal anti-inflammatory drugs) cardiovascular or haematological disorders, insulin resistance, diagnosed non-insulin dependent diabetes disease (Cardiovascular disease, heart failure, myocardial infarction, cerebrovascular disease, arteriosclerosis, diabetes, thyroid abnormality, ulcer, gastric bleeding, infectious diseases, systemic inflammatory diseases, acute inflammation, malignancy, renal disease, renal function, liver disease, lung disease, blood coagulopathy) take oriental medicine or other medicine during test period continuously subjects who have hypersensitivity about test material take fuctional foods continuously in the 4 weeks participate other human study in the 12 weeks pregnat woman or lactating woman subjects who unsuiable about this study

Design outcomes

Primary

MeasureTime frame
Platelet aggregation test

Secondary

MeasureTime frame
Blood flow;Lipids

Countries

Korea, Republic of

Contacts

Public ContactYeni Lim

Ewha Womans University

yeni0223@hanmail.net+82-2-3277-3087

Outcome results

None listed

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