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The effect of probiotic yogurt and regular yogurt consumption in patients with metabolic syndrome

Assessment of the effect of probiotic yogurt and regular yogurt consumption on the components, inflammatory and oxidative markers and vascular endothelial function in patients with metabolic syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201608213140N17
Enrollment
44
Registered
2016-11-09
Start date
2016-10-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrom. metabolic disorders not specified

Interventions

Intervention 1: Intervention group: 300 g/day probiotic yogurt including Lactobacillus acidophilus La5 and bifidobacterium lactis Bb12 for 8 weeks. Intervention 2: Placebo group: 300 g/day regular yog
Prevention
Placebo
Intervention group: 300 g/day probiotic yogurt including Lactobacillus acidophilus La5 and bifidobacterium lactis Bb12 for 8 weeks
Placebo group: 300 g/day regular yogurt

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Willingness to participate; women and men aged 20-65 years; diagnosis of the metabolic syndrome based on the presence of any 3 of the criteria defined by the Iranian National Committee of Obesity: waist circumference =95 cm in both genders; fasting serum glucose =100 mg/dl; serum triglyceride =150 mg/dl; serum HDL cholesterol <40 mg/dl in men and <50 mg/dl in women; systolic blood pressure =130 mmHg and/or diastolic blood pressure =85 mmHg. Exclusion criteria: suffering from cardiovascular disease, renal failure, diabetes and gastrointestinal diseases; receiving antibiotics; supplement of vitamin and minerals, fiber, omega-3 and probiotic supplements during the two months before the start of the study; presence of pregnancy or lactation or menopause; extreme sports more than 100 minutes per week; having the weight loss diet the three months before the study; hormone therapy; taking contraceptive drugs; alcohol intake, smoking and tobacco; history of cancer and medical treatment and drugs that affect the neuroendocrine function, metabolism or appetite; thyroid problems; gastrointestinal surgery during the past year; treatment with immunomodulatory drugs one month before the study; chronic use of laxative (more than twice a week).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood glucose. Timepoint: Begining and end of the intervention. Method of measurement: Enzymatic.;Insulin, insulin resistance index. Timepoint: Begining and end of the intervention. Method of measurement: ELISA and HOMA-IR formula.;Lipid profile. Timepoint: Begining and end of the intervention. Method of measurement: Spectrophotometry.;Blood pressure. Timepoint: Begining and end of the intervention. Method of measurement: Digital monometer.;Anthropometry markers. Timepoint: Begining and end of the intervention. Method of measurement: Stadiometer, scale, tape.;Tumor Necrosis Factor-Alpha (TNF-a). Timepoint: Begining and end of the intervention. Method of measurement: ELISA.;Interleukin-6 (IL-6). Timepoint: Begining and end of the intervention. Method of measurement: ELISA.;Hs-CRP. Timepoint: Begining and end of the intervention. Method of measurement: Immunotorbidometry.;Lipopolysaccharides (LPS). Timepoint: Begining and end of the intervention. Method of measurement: ELISA.;Malondialdehyde (MDA). Timepoint: Begining and end of the intervention. Method of measurement: Spectrophotometry.;Total Antioxidant Capacity. Timepoint: Begining and end of the intervention. Method of measurement: Spectrophotometry.;Uric Acid. Timepoint: Begining and end of the intervention. Method of measurement: Enzymatic.;Oxidized LDL (OxLDL). Timepoint: Begining and end of the intervention. Method of measurement: ELISA.;Plasminogen Activator Inhibitor-1 (PAI-1). Timepoint: Begining and end of the intervention. Method of measurement: ELISA.;Vascular Cell Adhesion Molecule Type 1 (VCAM-1). Timepoint: Begining and end of the intervention. Method of measurement: ELISA.;Intercellular Adhesion Molecule Type 1 (ICAM-1). Timepoint: Begining and end of the intervention. Method of measurement: ELISA.

Secondary

MeasureTime frame
Appetite. Timepoint: Begining and end of the intervention. Method of measurement: Appetite Questionnaire (Visual Analouge Scale).;Physical activity. Timepoint: Begining and end of the intervention. Method of measurement: International Physical Activity Questionnaire.;Energy and macronutrients intake. Timepoint: Begining and end of the intervention. Method of measurement: Three day dietary record questionnair.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Rezazadeh

Faculty of Nutrition and Food Sciences, Tabriz University of Medical Sciences

rezazadehl@tbzmed.ac.ir; rezazadehleila@yahoo.com+98 41 3335 7581

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 24, 2026