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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02622672
Other study ID # CS2-15095
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received November 19, 2015
Last updated March 13, 2017
Start date January 4, 2016
Est. completion date March 1, 2017

Study information

Verified date March 2017
Source Chung Shan Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Diabetes is considered an oxidative stress and a chronic inflammatory disease. Coenzyme Q10 (ubiquinone) is recognized as a lipid soluble antioxidant. Ubiquinol is a reduced form of coenzyme Q10 in our body after food or supplements intakes. Studies have indicated that the water-soluble ubiquinol had better antioxidant activity and absorption than lipid-soluble. The purpose of this study was to investigate the effects of a water-soluble ubiquinol supplement (100 mg/d) on antioxidation and anti-inflammation in diabetes patients.


Description:

The patients with type 2 diabetes will recruit as subjects (n = 50) and randomly assign to the placebo (n = 25) or coenzyme Q10 groups (n = 25). The intervention will administer for 12 weeks. The concentrations of coenzyme Q10, oxidative stress marker (malondialdehyde), antioxidant enzymes activities (superoxide dismutase, catalase, and glutathione peroxidase), inflammatory markers [C-reactive protein (CRP), and interleukin-6 (IL-6)], and biochemical parameters (fasting glucose, A1C, insulin, C-peptide, and lipid profiles), and blood pressure will measure. Hopefully, the results of this study could provide the information of water-soluble ubiquinol supplement for clinical doctors and dietitians recommend that diabetes patients deserve to know whether the use of coenzyme Q10 supplement.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 1, 2017
Est. primary completion date October 25, 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- The diagnostic criteria for type 2 diabetes were defined as a glycohemoglobin (A1C) ? 6.5%, a fasting glucose ? 7.0 mmol/L or a 2-h plasma glucose ? 200 mmol/L during an oral glucose tolerance test (OGTT), as well as the use of anti-hyperglycemic drugs.

Exclusion Criteria:

- pregnant or lactation women.

- patients with liver or renal disease

- Antioxidant dietary supplements user.

- patients under warfarin therapy.

- patients with hypoglycemia (fasting glucose < 60 mg/dL) or hyperlipidemia (fasting triglyceride ? 500 mg/dL)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
water-soluble ubiquinol
100 mg/d
Placebo
glycerin.soy-lecithin, and water

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yeh

Outcome

Type Measure Description Time frame Safety issue
Primary Fasting glucose serum level of fasting glucose in mmol/L. 12 weeks
Secondary Low density lipoprotein-cholesterol (LDL-C) serum level of LDL-C in mmol/L. 12 weeks
Secondary high density lipoprotein-cholesterol (HDL-C) serum level of HDL-C in mmol/L. 12 weeks
Secondary malondialdehyde (MDA) plasma level of MDA in micromol/L. 12 weeks
Secondary catalase (CAT) red blood cells level of CAT in Units/mg protein. 12 weeks
Secondary superoxide dismutase (SOD) red blood cells level of SOD in Units/mg protein. 12 weeks
Secondary glutathione peroxidase (GPx) red blood cells level of GPx in Units/mg protein. 12 weeks
Secondary high sensitivity C-reactive protein (hs-CRP) serum level of hs-CRP in mg/L. 12 weeks
Secondary high sensitivity interleukin (hs-IL-6) serum level of hs-IL-6 in pg/mL. 12 weeks
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