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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01099163
Other study ID # 2387
Secondary ID
Status Completed
Phase N/A
First received April 5, 2010
Last updated June 14, 2011
Start date January 2009
Est. completion date October 2010

Study information

Verified date April 2010
Source hahid Beheshti University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

Conjugated linoleic acids (CLAs) comprise a family of linoleic acid (18:2n-6; LA) isomers that are formed by biohydrogenation and oxidation processes in nature. The main form of CLA, cis-9, trans-11-18:2, can be produced directly by bacterial hydrogenation in the rumen or by delta-9 desaturation of the co-product vaccenic acid (trans-11-18:1) in most mammalian tissues including man. The second most abundant isomer of CLA is the trans-10, cis-12-18:2 form. Observations clearly emphasize that differences exist between mammalian species in their response to CLAs with mice being the most sensitive. The majority of studies on body compositional effects (i.e. fat loss, lean gain), on cancer and cardiovascular disease attenuation, on insulin sensitivity and diabetes and on immune function have been conducted with a variety of animal models. Recent studies indicate that some but not all of the effects observed in animals also pertain to human volunteers. Reports of detrimental effects of CLA intake appear to be largely in mice and due mainly to the trans-10, cis-12 isomer. Suggestions of possible deleterious effects in man due to an increase in oxidative lipid products (isoprostanes) with trans-10, cis-12 CLA ingestion require substantiation. Unresponsiveness to antioxidants of these non-enzymatic oxidation products casts some doubt on their physiological relevance. We hypothesized that supplementation with CLA + an antioxidant (vitamin E) in patients with diabetes mellitus may have beneficial effects on glycemic control and insulin sensitivity.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date October 2010
Est. primary completion date March 2010
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

- Diagnosis of type 2 diabetes mellitus > 5 years

- HbA1c = 9%

- Overweight or obese (BMI = 25 kg/m2 and = 30 kg/m2)

- Age = 30 and = 70 years (postmenopausal if female)

- Stable medical therapy for past 3 months

- Stable serum glucose for past 3 months (128-180 mg/Dl)

- Age between 30 to 50

- Use of metformin

- TG < 240 mg/Dl

- No alcohol, no insulin, no smoke

- No pregnancy, no menopause

Exclusion Criteria:

- Personal history of coronary heart disease

- Cerebrovascular disease or vascular disease

- Renal or hepatic disease

- Inflammatory diseases and thyroid diseases within the last years

- Use of drugs known to affect glycemic control, beta blockers, any change in daily activity profile, and diet

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care


Intervention

Dietary Supplement:
Tonalin SG1000T FFA


Locations

Country Name City State
Iran, Islamic Republic of Taleghani Hospital Tehran

Sponsors (1)

Lead Sponsor Collaborator
hahid Beheshti University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary insulin sensitivity No
Primary beta cell function
Primary glycosylated hemoglobin
Secondary inflammatory mediators (TNF-alpha, Il-1beta, Il-6, CRP, adiponectin, leptin)
Secondary systolic and diastolic blood pressure
Secondary serum lipids (TG, LDL, HDL, LDL/HDL, ApoB100)
Secondary fibrinogen, PAI-1
Secondary body fat using bioimpedance
Secondary oxidative stress (MDA)
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