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Effect of coenzyme Q10 supplementation on some biochemical factors in 2 diabetes

Effect of coenzyme Q10 supplementation on serum amylase ,adenosine deaminase, catalase, antioxidant capacity and lipid ratios in patients with type 2 diabetes

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016011325949N2
Enrollment
68
Registered
2016-01-25
Start date
2016-02-20
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

Type 2 diabetic. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention group: One capsule coenzyme Q10 (100 mg) per day for 12 weeks. Intervention 2: Control group: One capsule placebo cellulose acetate (100 mg) per day for 12 weeks.
Treatment - Drugs

Sponsors

Vice Chancellor for research of Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Type 2 diabetic patients for more than 2 years and not consumption of vitamin and mineral supplements during the last three months. Exclusion criteria: changing in dosage of glucose lowering medications; physical activity and diet during the intervention; any chronic renal; hepatic; thyroid; haematic; acute and chronic pancreatitis; tuberculosis; gastrointestinal disorders; using anticoagulants; diuretics and ß blockers; hormone therapy; insulin therapy; alcoholism; smoking; pregnancy and lactation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fasting glucose. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;Fasting insulin. Timepoint: Before and after 12 weeks of intervention. Method of measurement: ELISA.;HbA1C. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Chromatoghraphy.;TG. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;TC. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;HDL-C. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;LDL-C. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Friedewald’s equation.;Amylase. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;Adenosine deaminase. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;Catalase. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Spectrophotometric.;Antioxidant capacity. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Colorimetric.;Q10. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Chromatoghraphy.;Lipid ratios. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Formula.;Insulin sensitivity. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Formula.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Barometer.;Waist circumference. Timepoint: Before and after 12 weeks of intervention. Method of measurement: tape measure.;BMI. Timepoint: Before and after 12 weeks of intervention. Method of measurement: Formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ali Khosrowbeygi

Arak University of Medical Sciences

a.khosrowbeygi@arakmu.ac.ir; khosrowbeygi@yahoo.com+98 86 3417 3645

Outcome results

None listed

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