Determination of Glycemic Index (GI) of Ten Food Products
1 other identifier
interventional
15
1 country
1
Brief Summary
This study is initiated to investigate the glycemic index value of ten food products.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2012
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2012
CompletedFirst Submitted
Initial submission to the registry
August 30, 2012
CompletedFirst Posted
Study publicly available on registry
September 6, 2012
CompletedAugust 4, 2014
August 1, 2014
2 months
August 30, 2012
August 1, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
Glycemic index values of all ten products
Glycemic index values at 120 minutes post adminstration.
120 minutes post adminstration
Study Arms (1)
Food products
OTHERTen food products will be given to all subjects
Interventions
Eligibility Criteria
You may qualify if:
- Healthy non-pregnant females (at least 6 weeks postpartum, non-lactating)
- Age between 21 to 60 years
You may not qualify if:
- Suffering from any chronic diseases.
- Suffering from gastrointestinal diseases that may interfere with nutrient absorption, distribution, metabolism and excretion.
- History of diabtes mellitus or use of antihyperglycemic drugs or insulin to treat diabetes and related conditions.
- History of AIDS, hepatitis, renal or heart disease or any other serious complications that may interfere with glucose metabolism.
- Current use of medication that may interfere with the digestion and nutrient absorption (for examples steriods, protease inhibitors or antipsychotics medications).
- Current use of medication known to affect glucose tolerance (excluding oral contraceptives).
- Known food allergy or intolerance.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Temasek Polytechnic
Singapore, Singapore
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kalpana Bhaskaran, Dr
Temasek Polytechnic
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 30, 2012
First Posted
September 6, 2012
Study Start
February 1, 2012
Primary Completion
April 1, 2012
Study Completion
April 1, 2012
Last Updated
August 4, 2014
Record last verified: 2014-08