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Effects of coenzyme Q10 on paraxonase, total antioxidant capacity, malondialdehyde, hs-CRP, lipid profile and glycemic control in patients with type 2 diabetes

Effects of coenzyme Q10 on paraxonase, total antioxidant capacity, malondialdehyde, hs-CRP, lipid profile and glycemic control in patients with type 2 diabetes

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138806102394N1
Enrollment
50
Registered
2011-04-24
Start date
2009-11-06
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 diabetes. Non-insulin-dependent diabetes mellitus

Interventions

Intervention 1: Intervention group will receive daily 150 mg CoQ10 as three divided doses for 12 weeks. Each capsule consists of 50 mg CoQ10. Intervention 2: Placebo group will receive daily three cap
Treatment - Other
Placebo
Intervention group will receive daily 150 mg CoQ10 as three divided doses for 12 weeks. Each capsule consists of 50 mg CoQ10.
Placebo group will receive daily three capsules containing corn flour for12 weeks.

Sponsors

Vice-chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- Patients with type 2 diabetes 2- Willing to participate 3- Duration of type 2 diabetes > 1 year 4- HbA1c40 2- Past history of MI or stroke 3-Patients with any of the following conditions: liver disease, kidney disease, or thyroid disease 4-Supplement use for at least 8 weeks before intervention till the end of study 5- Treatment with warfarin 6-BP>160/90 7-Pregnancy and lactation 8-Compliance<70% 9-Change in type or dose of medication for at least 8 weeks before intervention till the end of study 10-Treatment with insulin

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Paraxonase. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: spectrophotometry.;Total antioxidant capacity. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: FRAP.;MDA. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: spectrophotometry.;Hs-CRP. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: turbidometry.;Triglyceride. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: Gop-PAP.;TC. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: enzymatic.;LDL. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: Friedewald formula.;HDL. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: precipitation.;HbA1c. Timepoint: before intervention, 12 weeks after intervention. Method of measurement: chromatography.

Secondary

MeasureTime frame
Insuline. Timepoint: before intervaention, 12 weeks after intervention. Method of measurement: RIA.;FBS. Timepoint: before intervaention, 12 weeks after intervention. Method of measurement: enzymatic.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 20, 2026