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Clinical Trials/IRCT201608299856N3
IRCT201608299856N3
Completed
Phase 2

Investigating the Effect of Synbiotic Supplementation and educating low-calorie diet on the Lipid Profile and the Gut Micro-flora in Patients with Metabolic Syndrome

Vice – Chancellery of Research & Technology Affairs of Kermanshah University of Medical Sciences0 sites132 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Condition 1: Hypertension. Condition 2: Hyperglyceridaemia. Condition 3: High-density lipoprotein deficiency.
Sponsor
Vice – Chancellery of Research & Technology Affairs of Kermanshah University of Medical Sciences
Enrollment
132
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Vice – Chancellery of Research & Technology Affairs of Kermanshah University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • Filling the consent form of the present project in the beginning of study; lack of any kinds of chronic diseases such as diabetes, renal diseases, tuberculosis, liver diseases and/or the history of cardiac surgeries; possessing at least 3 items of all the 5 indexes of metabolic syndrome (based on the definition by NCEP ATP III) (in case of insulin resistance, patients must have fasting blood glucose less than 126 mg/dL); lack of taking medication to control blood glucose, blood lipid and hypertension in the beginning of study ; the age range is between 25 to 65 year; lack of injecting/receiving insulin so as to blood glucose control in the beginning of study.
  • Exclusion criteria:
  • Lack of regular taking the given supplements; lack of following the given diet; starting taking medication or supplements that may be affect the results of test of investigated factors or oral contraceptives, estrogen, progesterone and corticosteroids; pregnancy; weaning, receiving insulin or tablet to control the blood glucose; losing any of inclusion criteria during the time of conducting the study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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