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Investigating the effects of zinc in reducing the risk of diabetes and cardiovascular diseases

Investigating the effect of zinc supplementation on the levels of oxidative stress and inflammation markers and glucose homeostasis in overweight or obese patients with metabolic syndrome

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240125060804N1
Enrollment
60
Registered
2024-01-31
Start date
2024-02-19
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Metabolic syndrome. Metabolic syndrome

Interventions

Intervention 1: Intervention group: Patients with metabolic syndrome receiving zinc supplementation. The dose of zinc received will be 30 mg orally once a day. Supplementation will be done for 12 week

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age over 18 to 70 years old Definite diagnosis of metabolic syndrome based on clinical symptoms and laboratory findings. Overweight or obesity (BMI above 25) Obtaining written informed consent from patients

Exclusion criteria

Exclusion criteria: Taking zinc supplements at least three months before starting the study The need to take blood sugar and lipid lowering drugs according to the doctor's opinion History of other diseases related to oxidative stress and inflammation such as cardiovascular diseases, autoimmune diseases, types of diabetes, IBD, asthma, cancer, kidney and liver diseases, Infectious diseases Smoking and alcohol consumption

Design outcomes

Primary

MeasureTime frame
Serum insulin. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Commercial ELISA kit.;Serum MDA. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: TBARS method.;Serum zinc. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Commercial spectrophotometry kit.;Serum total antioxidant capacity. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: FRAP method.;Serum lipid profile. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Commercial spectrophotometry kit.;Serum CRP. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Commercial kit.;Serum TNF-a. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Commercial ELISA kit.;HbA1C levels. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Commercial kit.;Serum fasting glucose. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Commercial kit.;Body Mass Index. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Scales, meter.;Waist circumference. Timepoint: Before the intervention, after the end of the intervention period. Method of measurement: Meter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMostafa Vaghari-Tabari

Mazandaran University of Medical Sciences

vagharim@tbzmed.ac.ir+98 11 3223 2963

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026