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Clinical Trials/KCT0002085
KCT0002085
Not yet recruiting
未知

A human study for investigating the effectiveness of Lactobacillus plantarum Q180 on control of triglyceride level

Chong Kun Dang Bio0 sites80 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Endocrine, nutritional and metabolic disease
Sponsor
Chong Kun Dang Bio
Enrollment
80
Status
Not yet recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Chong Kun Dang Bio

Eligibility Criteria

Inclusion Criteria

  • 1\) Subject who voluntarily agrees to participate and sign in informed consent form
  • 2\) Man and postmenopausal women (45 years \= Age )
  • 3\) Fasting triglyceride level \=150mg/dL and \<200mg/dL

Exclusion Criteria

  • 1\) Recommended Food Score \> 36
  • 2\) BMI \< 23kg/m2 or \> 35 kg/m2
  • 3\) high\-intensity exercise regularly (\=10 hours/week)
  • 4\) Chronic smokers (\=20cigarettes/day)
  • 5\) Alcoholics or drinking quantity: Alcohol 420g/week (soju about 7 bottles/week)
  • 6\) follwing disease or personal history
  • hyperlipidemia, diabetes mellitus, hypertension, liver complaint, enteropathy(including ulcerative colitis, lactose intolerance), renal disease, cardiovascular disease, cerebrovascular disease, pancreatitis, cancer, thyroid gland disease, dementia, Parkinson's disease, depressive disorder, anorexia nervosa/polyphagia, multiple sclerosis, Spinal cord injury
  • 7\) Volunteer who has taken follwing drug within 1\.5 months or during study period : Lipid Lowering Agent(Ursodeoxycholic acid, statin etc), antidiabetics, antibiotics, durg affecting Intestinal Functions, hormone, oral contraception, durg affecting lipid metabolism.
  • 8\) Volunteer who has taken herbal medicine within 2 months.
  • 9\) Volunteer who has taken probiotics, prebiotics, dietary supplements that affect the body fat, lipid metabolism or intestinal health within 1 months.

Outcomes

Primary Outcomes

Not specified

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