The effects of consumption of Lactobacillus Casei on diabetes control

Not Applicable

• Conditions: Diabetes Mallitus.; Non-insulin-dependent diabetes mellitus

• Registration Number: IRCT201607034105N17
• Lead Sponsor: Research Department of Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 44

Inclusion Criteria

Patients with diabetes for more than a year of developing diabetes and over 6 months pass the use of glucose lowering drugs ; Age 30 to 50 years. Exclusion criteria: Insulin injections; BMI> 35 Kg / m2; smoking; breastfeeding and pregnancy; menopause; using antibiotics and anti-inflammatory drugs within a month before and during the intervention; chronic digestive problems, and acute gastrointestinal problems within a month before and during the intervention; infectious and inflammatory diseases; Get any supplements.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Fasting Blood Sugar. Timepoint: befor intervention and after 2 monthes intervention. Method of measurement: Spectrophotometry.;HbA1c. Timepoint: befor intervention and after 2 monthes intervention. Method of measurement: Column chromatography.;Insulin Resistance. Timepoint: befor intervention and after 2 monthes intervention. Method of measurement: homeostasis model (HOMA-IR).;Serum Fetuin-A. Timepoint: befor intervention and after 2 monthes intervention. Method of measurement: ELISA technique.;Serum sirtuin1. Timepoint: befor intervention and after 2 monthes intervention. Method of measurement: ELISA technique.

Secondary Outcome Measures

Name	Time	Method
Height and Weight. Timepoint: Before Intervention and After2 Monthes Intervention. Method of measurement: Digital scale and stadiometer.;Food Intake. Timepoint: Before Intervention, Middle of the Intervention, and After Intervention. Method of measurement: 24-hour dietary recalls questionnaire.