Effect of Different Probiotic Strains in Hypercholesterolemic Patients
Hyperlipidemias
About this trial
This is an interventional treatment trial for Hyperlipidemias focused on measuring serum lipids, hyperlipidemia, probiotics
Eligibility Criteria
Inclusion Criteria:
• Had a repeated total cholesterol level ≥200 mg/dL prior to allocate to the study group and to declined conventional lipid lowering medical treatment
Exclusion Criteria:
- Those with any chronic conditions other than hypercholesterolemia,
- Individuals with inherited lipid metabolic disorders,
- Individuals with chronic gastrointestinal disease,
- Individuals with immunodeficiency,
- Individuals with malignancy,
- Individuals with mental disabilities,
- Patients currently using any lipid lowering drugs, or an alternative treatment to lower blood cholesterol (such as probiotics) and individuals who have used antibiotics in the previous three months prior to study and
- Pregnant or lactating women were excluded from the study.
Sites / Locations
- Gözde Okburan
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Placebo Comparator
Lactobacillus rhamnosus GG Group
Combined Lactobacillus acidophilus and Bifidobacterium animalis subsp.lactis Group
Placebo
Participants received only 1x106 cfu Lactobacillus rhamnosus GG once a day for 8 weeks.
Participants recevied a combined Lactobacillus acidophilus 1x109 cfu and Bifidobacterium animalis subsp.lactis 1x109 cfu once a day for 8 weeks.
Those participants received placebo capsule once a day for 8 weeks.