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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03242122
Other study ID # BL37 Part 1
Secondary ID
Status Completed
Phase N/A
First received July 31, 2017
Last updated August 31, 2017
Start date July 17, 2017
Est. completion date August 18, 2017

Study information

Verified date August 2017
Source Abbott Nutrition
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is open-label with a randomized, cross-over design using standard Gl methodology.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 18, 2017
Est. primary completion date August 18, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Subjects are males or non-pregnant females in good health.

- Subjects must be eligible to receive income in Canada and must demonstrate OHIP or equivalent medical coverage.

Exclusion Criteria:

- Subject with any type of food allergy or with a known history of AIDS, hepatitis, diabetes or a heart condition.

- Subject taking medication, or with any condition which might, in the opinion of the PI either make participation dangerous to the subject or to others or affect the results.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
CHO Control 1 and 2 Glucose
mixed in 237 ml/8 fl oz of a flavored non-caloric beverage; 1 time consumption
CHO Experimental 1 Slowly Digested
mixed in 237 ml/8 fl oz of a flavored non-caloric beverage; 1 time consumption
CHO Experimental 2 Digestion Resistant
mixed in 237 ml/8 fl oz of a flavored non-caloric beverage; 1 time consumption
CHO Experimental 3 Low Sugar
mixed in 237 ml/8 fl oz of a flavored non-caloric beverage; 1 time consumption
CHO Experimental 4 Maltodextrin
mixed in 237 ml/8 fl oz of a flavored non-caloric beverage; 1 time consumption

Locations

Country Name City State
Canada Glycemic Index Laboratories Inc Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
Abbott Nutrition

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood glucose response curve area under the curve (AUG) 0 to 120 minutes
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