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The Effect of Lactobacillus Reuteri on Lipid profile in Hypercholesterolemic Adults

Phase 3
Conditions
Hypercholesterolemia.
Dietary counseling and surveillance
Z71.3
Registration Number
IRCT20231111060016N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

THE AGE OF OUR participant will be between 20 to 70 years old; their total cholesterol plasma level will be above 200 mg/dl; HDL-C plasma level under 70 mg/dl; BMI will be between 20 to 45 kg/m2; they should sign informed consent

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The percentage of patients calculated by SCORE in each group had LDL with a suitable range for lifestyle modification, in the patients of Cardiovascular Clinic of Qaem Hospital. Timepoint: The lipid profile of the patients is measured before the start of the study, 30 days and then 60 days after taking the drugs. Method of measurement: Initial lipid profile testing.
Secondary Outcome Measures
NameTimeMethod
Secondary effects:1-Percentage of acute coronary syndrome (ACS: Unstable angina, NSTEMI, STEMI)2- Percentage of incidence of metabolic syndrome (by examining each metabolic syndrome criteria: abdominal circumference, fasting blood sugar level, HDL level, TG level, blood pressure level) in future monthly visits3. The percentage of LDL serum levels of patients after the study. Timepoint: Before starting the study, 30 days later and then 60 days after taking the capsules. Method of measurement: Description of oral condition in the form of an interview for the occurrence of ACS - use of sphygmomanometer to measure blood pressure - use of routine lipid profile tests and fasting blood sugar.
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