Status:
COMPLETED
Efficacy and Safety of Kochujang Pills on Blood Lipids Profiles in Hyperlipidemia Subjects
Lead Sponsor:
Chonbuk National University Hospital
Conditions:
Hyperlipidemia
Eligibility:
All Genders
19-55 years
Phase:
PHASE2
PHASE3
Brief Summary
The investigators performed a 12-week, randomized, double-blind, placebo-controlled human trial to evaluate the efficacy and safety of Kochujang pills on improvement of blood lipids. The investigators...
Eligibility Criteria
Inclusion
- Males and females 19-55 years old
- Total Cholesterol 200\~260 mg/dl or LDL-C 110\~190 mg/dl
- Able to give informed consent
Exclusion
- Allergic or hypersensitive to any of the ingredients in the test products
- History of reaction to any of the test products or of gastrointestinal diseases such as Crohn's disease or gastrointestinal surgery
- History of alcohol or substance abuse
- Participation in any other clinical trials within past 2 months
- Laboratory test, medical or psychological conditions deemed by the investigators to interfere with successful participation in the study
- Pregnant or lactating women etc.
Key Trial Info
Start Date :
November 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2012
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT01865370
Start Date
November 1 2011
End Date
April 1 2012
Last Update
May 30 2013
Active Locations (1)
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1
Clinical Trial Center for Functional Foods; Chonbuk National University Hospital
Jeonju, Jeollabuk-do, South Korea, 560-822