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Study of oral zinc supplementation effect on type 2 diabetes

Study of oral zinc supplementation effect on the superoxide dismutase gene expression and enzyme activity, and oxidative stress index in overweight type 2 diabetic patients.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150831023838N1
Enrollment
70
Registered
2018-01-05
Start date
2018-01-06
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Type 2 diabetes mellitus. Type 2 diabetes mellitus

Interventions

Intervention 1: Intervention group: One day will take, 2 capsules of zinc gluconate 25 mg for 60 days. These capsules are made by ALHAVI Company in Iran. Intervention 2: Control group: One day will ta

Sponsors

Endocrinology and metabolism research institute
Lead Sponsor
Tarbiat Modares university faculty of medical sciences
Collaborator

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: Afflicted with type 2 diabetes mellitus BMI= 25-30 kg/m2 HbA1c =7

Exclusion criteria

Exclusion criteria: Smoking Taking diuretics Taking antibiotics Taking multivitamins containing zinc Gastrointestinal disorders Thyroid disorders Cancer history Renal disorders Liver disorders

Design outcomes

Primary

MeasureTime frame
Gene expresion of Superoxide dismutase. Timepoint: Before and 8 weeks after intervention. Method of measurement: Real time PCR.;Superoxide dismutase activity. Timepoint: Before and 8 weeks after intervention. Method of measurement: ELISA.;Serum levels of Zinc. Timepoint: Before and 8 weeks after intervention. Method of measurement: Atomic Absorption Spectroscopy.;Serum levels of Malondialdehyde. Timepoint: Before and 8 weeks after intervention. Method of measurement: ELISA.;Serum levels of Total Antioxidant Capacity. Timepoint: Before and 8 weeks after intervention. Method of measurement: ELISA.;Serum levels of Total Oxidant Capacity. Timepoint: Before and 8 weeks after intervention. Method of measurement: ELISA.;Serum levels of Nitrotyrosine. Timepoint: Before and 8 weeks after intervention. Method of measurement: ELISA.;Serum levels of Fasting Blood Suger. Timepoint: Before and 8 weeks after intervention. Method of measurement: spectroscopy.;Glycated hemoglobin. Timepoint: Before and 8 weeks after intervention. Method of measurement: High Efficiency Liquid Cgromotography (HPLC).;Serum levels of Cholestrol. Timepoint: Before and 8 weeks after intervention. Method of measurement: spectroscopy.;Serum levels of Triglycerid. Timepoint: Before and 8 weeks after intervention. Method of measurement: spectroscopy.;Serum levels of Insulin. Timepoint: Before and 8 weeks after intervention. Method of measurement: Electrochemiluminescence.;Height. Timepoint: Before the intervention. Method of measurement: Meter.;Weight. Timepoint: Before and 8 weeks after intervention. Method of measurement: Scales.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojgan Asadi

Tehran University of Medical Sciences

asadim@tums.ac.ir+98 21 8863 1298

Outcome results

None listed

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