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Glycemic Response Testing

M

Mondelez International

Status

Completed

Conditions

Glycemic Index
Glycemic Response

Treatments

Other: Dietary Intervention

Study type

Interventional

Funder types

Industry

Identifiers

NCT01536860
P12-00794

Details and patient eligibility

About

The purpose of this study is to assess whether added food ingredient(s) affect glycemic responses to a liquid meal tolerance test (LMTT).

Enrollment

12 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% males or females
  • Non-smoker
  • Aged 18 to 55 years
  • Have a body mass index between 18.5 to 29.99 kg/m2
  • Healthy, non-diabetic, no gastric bypass surgery
  • Not allergic to mustard, dairy or soy
  • Having 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

12 participants in 3 patient groups, including a placebo group

Control Test Drink
Placebo Comparator group
Description:
control drink
Treatment:
Other: Dietary Intervention
Other: Dietary Intervention
Other: Dietary Intervention
Experimental Test Drink 1
Experimental group
Description:
control drink containing ingredient 1
Treatment:
Other: Dietary Intervention
Other: Dietary Intervention
Other: Dietary Intervention
Experimental Test Drink 2
Experimental group
Description:
Control drink containing ingredient 2
Treatment:
Other: Dietary Intervention
Other: Dietary Intervention
Other: Dietary Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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