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The effects of glutamine supplementation in type 2 diabetes

The effects of glutamine supplementation on lipid profile, inflammatory and metabolic factors in type 2 diabetes.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205279373N1
Enrollment
60
Registered
2012-08-13
Start date
2012-08-25
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

Diabetes mellitus. Non-insulin dependent diabetes mellitus

Interventions

Intervention 1: glutamine ( 3 times a day for 6 weeks). Intervention 2: cellulose (3 times a day for 6 weeks).
Treatment - Drugs
glutamine ( 3 times a day for 6 weeks)
cellulose (3 times a day for 6 weeks)

Sponsors

Endocrinology & Metabolism Research Institute, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patient diagnosed with type 2 diabetes based on ADA definition or who only take oral antidiabetic drug Exclusion criteria: history of drug dependence; body mass index (BMI) =35 kg/m2; history of cancer; treatment with anti-inflammatory; corticosteroid; hormonal or antibiotic agents; a restrictive diet or weight change = 5 kg during the 3months prior to study; systolic blood pressure >160 mmHg and/or diastolic blood pressure > 90 mmHg; fatty liver disease; liver or kidney disease; autoimmune disease; pregnancy and lactation; any change in treatment with oral hypoglycemic; anti hypertensive and antilipid agents during the study; use of weight loss medications; HbA1C >8

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Fast blood sugar. Timepoint: Before and 6 weekes after the intervention. Method of measurement: mg/ dl / enzymatic.;GLP-1 ( Glucagon- like peptide-1). Timepoint: Before and 6 weekes after the intervention. Method of measurement: pmol/ l / ELISA.;Serum insulin. Timepoint: Before and 6 weekes after the intervention. Method of measurement: pmol/ l / IRMA method.;Serum c peptide. Timepoint: Before and 6 weekes after the intervention. Method of measurement: mg/ l.;Hs- CRP. Timepoint: Before and 6 weekes after the intervention. Method of measurement: ELSA.;Resting energy expenditure. Timepoint: Before and 6 weekes after the intervention. Method of measurement: indirect calorimetry.

Secondary

MeasureTime frame
Srum glutamine. Timepoint: Before and 6 weekes after the intervention. Method of measurement: spectrophotometric.;Blood pressure. Timepoint: Before and 6 weekes after the intervention. Method of measurement: blood pressure,sphygmomanometer.;Total cholestrol. Timepoint: Before and 6 weekes after the intervention. Method of measurement: mg/ dl.;HDL-C. Timepoint: Before and 6 weekes after the intervention. Method of measurement: mg/ dl.;LDL-C. Timepoint: Before and 6 weekes after the intervention. Method of measurement: mg/dl.;Hb A1C. Timepoint: Before and 6 weekes after the intervention. Method of measurement: fast HbA1c serum level,Chromatography.;Serum creatinine. Timepoint: Before and 6 weekes after the intervention. Method of measurement: mg/dl.;Body composition. Timepoint: Before and 6 weekes after the intervention. Method of measurement: Tanita body composition analyzer.;Triglyceride. Timepoint: Before and 6 weekes after the intervention. Method of measurement: mg/dl.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAsieh Mansour

Endocrinology & Metabolism Research Institute Tehran University of Medical Sciences

asiehmansour@yahoo.com+882 20037

Outcome results

None listed

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