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8 weeks, single-center, randomized, double-blind, placebo-controlled clinical trial for the evaluation of the efficacy and safety of Rubus coreanus extract on inhibition of platelet aggregation and blood coagulatio

Not Applicable
Recruiting
Conditions
Not Applicable
Registration Number
KCT0000915
Lead Sponsor
ee’s Biotech
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
80
Inclusion Criteria

1) male smoker aged not less then 20 years averagely consuming 10 cigarettes per day.
2) not less then 70% of Platelet aggregation.
3) People who sign the informed consent form before participating in the study

Exclusion Criteria

1) subject with clinically significant myocardial infarction, angina pectoris,hemorrhagic lesion, cardiovascular disease under current medication or treatment
2) subject who has taken aspirin, anticoagulant, antiplatelet agent within 2 weeks
3)subject who has taken health functional food such as antioxidant(vitamin C, E), red ginseng , ginseng , chongkukjang, natto within 2 weeks
4)subject under treatment for uncontrolled hypertension
(over 160/100 mmHg)
5)subject under treatment for uncontrolled diabetes (fasting plasma glucose 180mg/dl or diabetes patient starting drugs within 3 months)
6)subject under treatment for thyroid disease etc. (However, subjects can be involved in the study based on doctor’s assessment)
7)subject with operation medical history within 3 months
8)subject whose creatinine level is twice higher than the normal range
9)subject whose AST(GOT) or ALT(GPT) level is three times higher than normal range
10)people complaining of a heartburn,dyspepsia, severe gut symptoms
11)subject scheduled for participating in another study during this study period or who had participated in other study within 3 months
12)subject who investigators think is not suitable for this study.

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Platelet aggregation
Secondary Outcome Measures
NameTimeMethod
lipid test;C-reactive protein ;blood coagulation test
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