- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01952977
Effect of Medium Chain Triglyceride Consumption on Appetite (MCT)
September 27, 2013 updated by: Marie-Pierre St-Onge, St. Luke's-Roosevelt Hospital Center
The purpose of this study is to test the effects of medium chain triglyceride consumption, relative to long chain triglycerides, on hormones involved in appetite regulation and food intake in overweight men.
We expect medium chain triglycerides to reduce appetite and food intake and to do so by increasing levels of hormones known to be involved in satiety and reduce levels of those involved in appetite.
Study Overview
Study Type
Interventional
Enrollment (Actual)
17
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10025
- New York Obesity Nutrition Research Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 50 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Males
- Weight stable (<10 lb over previous 3 months)
- Overweight (body mass index 25-29.9)
Exclusion Criteria:
- Smokers
- Excessive caffeine users
- Severe health conditions
- Allergy to food products/ingredients in the study
- Taking medications known to affect energy expenditure or gastrointestinal function
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: MCT
MCT oil (20 g) was included in the test breakfast
|
|
|
PLACEBO_COMPARATOR: LCT
Corn oil (20 g) was included in the test breakfast
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Food intake
Time Frame: up to 3 hours
|
Intake at an ad libitum meal 3 h after test oil consumption (Study 1) or 1 h after a pre-load containing the test oil (Study 2)
|
up to 3 hours
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Ghrelin
Time Frame: 3 hours
|
3 hours
|
|
Peptide YY
Time Frame: 3 hours
|
3 hours
|
|
Glucagon-like peptide 1
Time Frame: 3 hours
|
3 hours
|
|
Insulin
Time Frame: 3 hours
|
3 hours
|
|
Triglycerides
Time Frame: 3 hours
|
3 hours
|
|
Leptin
Time Frame: 3 hours
|
3 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Marie-Pierre St-Onge, Ph.D, New York Obesity Nutrition Research Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2010
Primary Completion (ACTUAL)
August 1, 2011
Study Completion (ACTUAL)
August 1, 2011
Study Registration Dates
First Submitted
September 25, 2013
First Submitted That Met QC Criteria
September 27, 2013
First Posted (ESTIMATE)
September 30, 2013
Study Record Updates
Last Update Posted (ESTIMATE)
September 30, 2013
Last Update Submitted That Met QC Criteria
September 27, 2013
Last Verified
September 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- MCT_1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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