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Clinical Trials/KCT0000259
KCT0000259Completed未知

Effect of four weeks consumption of chlorella on cholesterol levels in mildly hypercholesterolemic adults : a randomized, double-blind, controlled study

Ewha Womans University0 sites68 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Completed
Enrollment
68

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional Study

Eligibility Criteria

Ages
20(Year) to o Limit (—)
Sex
All

Inclusion Criteria

  • 1) Voluntarily agree to participate and signed in informed consent form
  • 2) Adults aged over 20 years
  • 3) Plasma total cholesterol levels = 200mg/dl and < 250mgl/dl

Exclusion Criteria

  • 1) Continuous consumption of drug or dietary supplement that affect lipid metabolism within 4 weeks before the first visit (statin, fibrate, beta-blocker, etc)
  • 2) Following diseases:
  • ? Myocardial infarction, stroke, uncontrolled hypertension (= 140/90mmHg)
  • ? Diabetes (fasting plasma glucose = 126mg/dl)
  • ? Liver failure(AST, ALT rose more than 2.5 times the upper limit of normal)
  • ? Renal impairment (Creatinine = 1.4mg/dl)
  • ? Hyperthyroidism and hypothyroidism
  • ? Malignant tumors
  • 3) Familial hypercholesterolemia
  • 4) Participation in another clinical trial within 4 weeks of first visit
  • 5) Alcoholic
  • 6) Pregnant or lactating women
  • 7) Hypersensitivity to chlorella
  • 8) Any condition that the principal investigator belives may put the subjects at undue risk

Investigators

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