An interventional study of cinnamon in Normal Weight and Overweight and Obesity, sponsored by University of California, Los Angeles. Completed at 1 site in United States. Open to participants aged 20 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-12-28.
Sponsored by University of California, Los Angeles · Not applicable, Interventional, and Treatment
The objective of the proposed study is to investigate the effect of cinnamon on the postprandial glycemic response to a high glycemic index meal in normal and overweight/obese prediabetic subjects
A randomized crossover study design will be carried out in accordance with the guidelines of the Human Subjects Protection Committee of the University of California, Los Angeles. All subjects will give written informed consent before the study begins. There will be two groups of participants (normal and overweight/obese). Each participant will consume oatmeal prepared with 1 cup of 2% milk served with or without 6 g of ground cinnamon in random sequence. At each meal consumption blood will be collected to measure postprandial glucose and insulin at 0, 30, 60, 90, 120, 150 and 180 minutes.
3,670 studies on the registry are indexed under Overweight; 849 are open to participants now.
This study's enrollment of 32 is below the median of 73 across 3,175 interventional studies indexed under Overweight.
Browse Overweight studies →University of California, Los Angeles is the lead sponsor of 1,142 studies on the registry; 192 are open to participants now.
Of its 91 completed or terminated interventional studies of FDA-regulated products, 66 (73%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
The test meal consisted of ½ cup dry instant oatmeal, prepared with 1 cup of 2% milk served with 6 g of ground cinnamon.
Dietary Supplement: cinnamon
The test meal consisted of ½ cup dry instant oatmeal, prepared with 1 cup of 2% milk served without 6 g of ground cinnamon
6 g of ground cinnamon
Also known as: control
glucose
postprandial glucose reponse
Time frame: Baseline to 180 minutes
insulin
postprandial insulin response
Time frame: Baseline to 180 minutes
C-peptide
postprandial C-peptide response
Time frame: Baseline to 180 minutes
glucagon
postprandial glucagon reponse
Time frame: Baseline to 180 minutes
lipids
postprandial lipid response
Time frame: Baseline to 180 minutes
This study is completed, as verified in Dec 2020. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
University of California, Los Angeles