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The Effect of Oral Powder Enriched with Curcumin and Probiotics on Patients with Metabolic Syndrome

Phase 3
Conditions
Metabolic syndrome.
Metabolic syndrome
E88.81
Registration Number
IRCT20220315054290N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
124
Inclusion Criteria

Age: 30-60 years old
Metabolic syndrome patients are diagnosed based on the Adult Treatment Panel III (ATP III) criterion
Consent to participate in the study

Exclusion Criteria

Pregnancy
Lactation
Suffering from kidney, liver, and systemic diseases at the beginning of the study
Metabolic, endocrine, and cardiovascular diseases except diabetes, dyslipidemia, and hypertension
Take any supplements or antibiotics during the previous 3 months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
eptin hormone. Timepoint: Before the study and 8 weeks after the start of the study. Method of measurement: Leptin kit (ELISA).;Ghrelin hormone. Timepoint: Before the study and 8 weeks after the start of the study. Method of measurement: Ghrelin kit (ELISA).;Appetite. Timepoint: Before the study and 8 weeks after the start of the study. Method of measurement: Visual Analog Scale (VAS) questionnaire.
Secondary Outcome Measures
NameTimeMethod
Weight. Timepoint: Before the intervention and 8 weeks after the start of the intervention. Method of measurement: Scale.;Waist circumference. Timepoint: Before the intervention and 8 weeks after the start of the intervention. Method of measurement: Inelastic tape.;Body fat percentage. Timepoint: Before the intervention and 8 weeks after the start of the intervention. Method of measurement: Body analyzer device.
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