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Glycaemic Response Testing

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ClinicalTrials.gov Identifier: NCT01536847
Recruitment Status : Completed
First Posted : February 22, 2012
Last Update Posted : September 10, 2012
Sponsor:
Collaborator:
Information provided by (Responsible Party):

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

Condition or disease Intervention/treatment
Glycaemic Index Glycaemic Response Other: Dietary Intervention

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 12 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single (Participant)
Primary Purpose: Basic Science
Official Title: Glycaemic Response Testing
Study Start Date : December 2011
Primary Completion Date : January 2012
Study Completion Date : January 2012
Arms and Interventions

Arm Intervention/treatment
Placebo Comparator: Control Test Drink
Control drink
Other: Dietary Intervention
300 ml of liquid food product
Experimental: Experimental Test Drink 1
Control drink containing ingredient 1
Other: Dietary Intervention
300 mL of liquid food product
Experimental: Experimental Test Drink 2
Control drink containing ingredient 2
Other: Dietary Intervention
300 ml of liquid food product


Outcome Measures

Primary Outcome Measures :
  1. Glycaemic index of experimental test food using capillary blood [ Time Frame: 0-120 minutes ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
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
  • Having a fasting plasma glucose (finger stick) <100 mg/dl (<5.5 mmol/L)
  • Willing and able to provide written informed consent
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01536847


Sponsors and Collaborators
Mondelēz International, Inc.
Reading Scientific Services Ltd.
Investigators
Principal Investigator: Suzana Louth, Dr RSSL
More Information

Responsible Party: Mondelēz International, Inc.
ClinicalTrials.gov Identifier: NCT01536847     History of Changes
Other Study ID Numbers: P11-09257
First Posted: February 22, 2012    Key Record Dates
Last Update Posted: September 10, 2012
Last Verified: September 2012