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Glycaemic Responses to Cracker Snacks

M

Mondelez International

Status

Completed

Conditions

Glycaemic Response Measurements

Treatments

Other: Experimental Cracker Snack 1
Other: Control Cracker Snack
Other: Experimental Cracker Snack 2

Study type

Interventional

Funder types

Industry

Identifiers

NCT01687569
P12-05774

Details and patient eligibility

About

The purpose of this study is to determine whether added ingredient affects glycaemic responses to a cracker snack.

Enrollment

27 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Male or female (not less than 40% Male)
  • Aged 18 - 55 years
  • Non Smokers
  • Have a body mass index between 18.5 to 29.99 kg/m2
  • Healthy, non-diabetic, no gastric bypass surgery
  • Not allergic to wheat, mustard, dairy, or soy
  • Have a fasting plasma glucose (finger-stick) <100 mg/dl (<5.5 mmol/L)
  • Willing and able to provide written informed consent

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

27 participants in 3 patient groups, including a placebo group

Control Cracker
Placebo Comparator group
Description:
Base cracker snack
Treatment:
Other: Control Cracker Snack
Experimental Cracker Snack 1
Experimental group
Description:
Cracker snack containing test ingredient 1
Treatment:
Other: Experimental Cracker Snack 1
Experimental Cracker Snack 2
Experimental group
Description:
Cracker snack containing test ingredient 2
Treatment:
Other: Experimental Cracker Snack 2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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