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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03667963
Other study ID # RIS protocol number 33593
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 29, 2018
Est. completion date December 21, 2018

Study information

Verified date January 2019
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the effect of different methods of preparation (cooked and consumed hot vs cooked, cooled overnight and consumed cold) and variation in the activity of salivary amylase on the glycemic index and carbohydrate digestibility in healthy human subjects. The effect of genetic variation in small intestinal starch digesting enzymes on glycemic index and starch digestibility will also be assessed.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 21, 2018
Est. primary completion date December 21, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Males or non-pregnant females aged 18-75 years and in good health

- Eligible to receive income in Canada

- Have Ontario Health Insurance Plan or equivalent medical coverage.

- Previous donor of saliva using protocol reference number # 31093 or GIL-1670 (in which subject consents to measurement of salivary amylase activity and genetic variation in AMY1, SI and MGAM genes).

- Salivary amylase activity in the lowest tertile (<50 U/ml) or highest tertile (>105 U/ml) of salivary amylase activity of 40 subjects previously measured.

Exclusion Criteria:

- known history of AIDS, hepatitis, diabetes or a heart condition

- Allergy to rice, canola oil or sesame oil.

- use of medications (including, but not limited to, insulin or other antidiabetic drugs, systemic steroids, antipsychotics, protease inhibitors, antivirals, immunosuppressive agents and drugs affecting gut motility or digestion) or with any condition which might, in the opinion of Dr. Wolever, the Medical Director or GI Labs, either: 1) make participation dangerous to the participant himself (or herself) or to others, or 2) affect the results.

- individuals who cannot or will not comply with the experimental procedures or do not follow the instructions of GI Labs staff related to the safe performance of the experimental procedures

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Glucose
50g glucose dissolved in 250ml water
Glucose plus lactulose
50g glucose plus 10g lactulose dissolved in 250ml water
Hot Rice
Freshly cooked polished rice containing 50g available carbohydrate (approximately 2/3 cup cooked rice) and consumed hot.
Cold Rice
Cooked polished rice containing 50g available carbohydrate (approximately 2/3 cup cooked rice) cooled overnight in a refrigerator and consumed cold.

Locations

Country Name City State
Canada Glycemic Index Laboratories Toronto Ontario

Sponsors (2)

Lead Sponsor Collaborator
University of Toronto Glycemic Index Laboratories, Inc

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Glycemic Index (GI) For each subject, the incremental area under the glucose response curve over 2 hours (iAUC) after each rice test meal is expressed as a percentage of the mean iAUC elicited by the 2 glucose test meals. 0-2 hours
Secondary Carbohydrate malabsorbed For each test meal the sum of breath hydrogen concentrations from the lowest value over 0-3 hours to 6 hours (termed "H"). For each subject the amount of hydrogen per gram malabsorbed carbohydrate (H/g) is calculated as (GL-G)/10 where GL is H after the glucose plus lactose meal and G is H after the glucose meal. The amount of carbohydrate malabsorbed after the hot and cold rice meals, respectively, are HR/Hg and CR/Hg, where HR and Cr are H after the hot and cold rice meals. 0-6 hours.
Secondary Glycemic response The incremental area under the blood glucose response curve 0-2 hours
Secondary Breath hydrogen response Sum of breath hydrogen concentrations from the lowest in the first 3 hours to 6 hours. 0-6 hours
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