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Effect of Intake of Citron(Citrus Junos Siebold ex Tanaka) Peel Extract on Blood Cholesterol.

Not Applicable
Completed
Conditions
Hyperlipidemia
Interventions
Dietary Supplement: Citron peel extract
Dietary Supplement: Placebo
Registration Number
NCT03332641
Lead Sponsor
Hanyang University
Brief Summary

This study was conducted to investigate the effects of daily supplementation of Citron(Citrus Junos Siebold ex Tanaka) Peel Extract on improvement of Blood Cholesterol.

Detailed Description

This study was a 12 weeks, randomized, double-blind, placebo-controlled human trial. Twenty subjects were randomly divided into Citron(Citrus Junos Siebold ex Tanaka) Peel Extract or a placebo group. Blood cholesterol profiles before and after the intervention.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
70
Inclusion Criteria
  • Age 19-75 years with Total cholesterol 200-239 mg/dL
Exclusion Criteria
  • Lipid lowering agent within past 6 months
  • Severe cardiovascular disease(Mvodardial infarction, stroke, etc)
  • Renal disease(Heredity hyperlipidemia, Acute/Chronic renal failure, Nephrotic syndrome, ect)
  • Cancer, Respiratory organ disease(Asthma, Chronic obstructive pulmonary disease)
  • Diabetes mellitus
  • Allergic or hypersensitive to any of the ingredients in the test products
  • History of disease that could interfere with the test products or impede their absorption
  • Under antipsychotic drugs therapy within past 2 months
  • History of alcohol or substance abuse
  • Participation in any other clinical trials within past 2 months
  • Laboratory test by show the following results
  • Pregnancy or breast feeding
  • Not Contraception(except: Surgery for female infertility)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Citron peel ExtractCitron peel extractCitron peel extract for 12 weeks
PlaceboPlaceboPlacebo for 12 weeks
Primary Outcome Measures
NameTimeMethod
Changes of Cholesterol12 weeks

Changes of Cholesterol were assessed before and after the intervention

Secondary Outcome Measures
NameTimeMethod
Changes of Lipid profile12 weeks

Changes of Lipid profile were assessed before and after the intervention

Changes of Oxidized LDL12 weeks

Changes of Oxidized LDL were assessed before and after the intervention

Trial Locations

Locations (1)

Hanyang University

🇰🇷

Seoul, Korea, Republic of

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