Status:
COMPLETED
Blood Glucose Response to Highly Viscous Polysaccharide Enriched Biscuits in Healthy and Diabetic Subjects
Lead Sponsor:
Unity Health Toronto
Conditions:
Type 2 Diabetes
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief Summary
Our objective was to test whether the highly viscous polysaccharide incorporated into the biscuit formulation would reduce the postprandial blood glucose response equally in healthy subjects and indiv...
Detailed Description
Despite significant achievements in treatment modalities and preventive measures, diabetes has been increasing exponentially. Reduction in both fasting and prolonged postprandial glycemia is of paramo...
Eligibility Criteria
Inclusion
- Inclusion Criteria (arm 1):
- males or non-pregnant females aged 18-75 years and in good health;
- BMI \<30 kg/m2.
- Exclusion Criteria (arm 1):
- known history of hepatitis, diabetes or a heart condition;
- using medications or fiber supplements;
- any health condition which might affect the results;
- non-compliance with the experimental procedures.
- Inclusion Criteria (arm 2):
- documented type 2 diabetes for at least 6 month duration without clinically manifest complications;
- age 18-75 years;
- BMI \<30 kg/m2.
- Exclusion Criteria (arm 2):
- liver or kidney disease;
- gastrointestinal problems;
- using fiber supplements;
- non-compliance with the experimental procedures;
- pregnancy.
Exclusion
Key Trial Info
Start Date :
August 1 1989
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 1989
Estimated Enrollment :
19 Patients enrolled
Trial Details
Trial ID
NCT00728143
Start Date
August 1 1989
End Date
November 1 1989
Last Update
August 5 2008
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.