CTRI/2017/06/008903
Active, not recruiting
未知
A randomized, double blind, controlled clinical trial to assess the Efficacy and safety of liposomal Curcumin compared with Curcumin (non-liposomal) on inflammation in subjects with metabolic syndrome
CureSupport0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Metabolic syndrome
- Sponsor
- CureSupport
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. 18 years of age and above
- •2\. Metabolic abnormalities with or without alcohol consumption and/or smoking
- •3\. Diagnosis of MetS ie. the presence of three or more criteria of the modified National Cholesterol Education Programs Adult Treatment Panel III ( NCEP ATP III):
- •3\.1 Waist circumference 90 cm in men and 80 cm in women
- •3\.2 Hypertriglyceridemia \>\= 150 mg/dl
- •3\.3 High density lipoprotein (HDL) cholesterol 40 mg/dl in males and 50 mg/dl in females
- •3\.4 Blood pressure \>\= 130/85 mm Hg
- •3\.5 Fasting plasma glucose \>\= 110 mg/dl
- •4\.0 Patients willing to provide written informed consent
Exclusion Criteria
- •1\. Pregnancy or breastfeeding,
- •2\. lack of compliance with the study medication (defined as not using the medication for \>1 week),
- •3\. Participation in a concomitant trial,
- •4\. Hypersensitivity to the study medication,
- •5\. Presence of malignancies
- •6\. Impossibility to give informed consent.
- •7\. Intake of drugs or dietary supplements
- •8\. Previous illnesses such as heart attack, cancer or dementia
- •9\. Addiction illness
Outcomes
Primary Outcomes
Not specified
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