The safety and effect of a new sweetener (Lacritose) compared to sugar and glucose on postprandial blood sugar
Phase 2
- Conditions
- on-insulin-dependent diabetes mellitus.non insulin dependent diabetes mellitus
- Registration Number
- IRCT2015050912571N2
- Lead Sponsor
- Vice chancellor for research, Shahid Sadoughi University of Mecical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Type 2 diabetic patients (n=20) with fasting blood sugar >125 mg/dl and lower than 200 mg/dl, aged 20 to 60.
Exclusion criteria:
Participants will not be included in the trial if they were pregnant or lactating, had severe infection, endocrine disorders or acute diseases at the enrollment. Participants who intend to exit with any reasons or show any adverse reaction to test sugars will also be excluded from the study. .
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postprandial blood sugar. Timepoint: Every 30 minutes up to 2 hours after ingesting the test beverages. Method of measurement: Using pars azmoon kits using automated azalyzer.
- Secondary Outcome Measures
Name Time Method Gastrointestinal symptoms. Timepoint: 24 hour after ingesting the test beverages. Method of measurement: Gastrointestinal symptoms questionnaire.