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Clinical Trials/NCT03242122
NCT03242122CompletedNot Applicable

Evaluation of Carbohydrates

Abbott Nutrition1 site in 1 country10 target enrollmentStarted: July 17, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Blood glucose response curve

Study Overview

Brief Summary

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

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Arms & Interventions

CHO Control 1 Glucose

Active Comparator

25 g glucose

Intervention: CHO Control 1 and 2 Glucose (Other)

CHO Experimental 1 Slowly Digested

Experimental

25 g slowly-digested carbohydrate blend

Intervention: CHO Experimental 1 Slowly Digested (Other)

CHO Experimental 2 Digestion Resistant

Experimental

25 g digestion-resistant carbohydrate blend

Intervention: CHO Experimental 2 Digestion Resistant (Other)

CHO Experimental 3 Low Sugar

Experimental

25 g low sugar carbohydrate blend

Intervention: CHO Experimental 3 Low Sugar (Other)

CHO Experimental 4 Maltodextrin

Experimental

25 g maltodextrin

Intervention: CHO Experimental 4 Maltodextrin (Other)

CHO Control 2 Glucose

Active Comparator

25 g glucose

Intervention: CHO Control 1 and 2 Glucose (Other)

Outcomes

Primary Outcomes

Blood glucose response curve

Time Frame: 0 to 120 minutes

area under the curve (AUG)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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