The Role of the Endocannabinoid System in Sweet Taste Intensity and Liking
NCT ID: NCT02112292
Last Updated: 2017-05-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2014-04-30
2015-04-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
BASIC_SCIENCE
TRIPLE
Study Groups
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T-C-P
Order of administrations: tetrahydrocannabinol - cannabidiol - placebo
tetrahydrocannabinol
cannabidiol
Placebo
T-P-C
Order of administrations: tetrahydrocannabinol - placebo - cannabidiol
tetrahydrocannabinol
cannabidiol
Placebo
C - T - P
Order of administrations: cannabidiol - tetrahydrocannabinol - placebo
tetrahydrocannabinol
cannabidiol
Placebo
C - P - T
Order of administrations: cannabidiol - placebo - tetrahydrocannabinol
tetrahydrocannabinol
cannabidiol
Placebo
P - T - C
Order of administrations: placebo - tetrahydrocannabinol - cannabidiol
tetrahydrocannabinol
cannabidiol
Placebo
P - C - T
Order of administrations: placebo - cannabidiol - tetrahydrocannabinol
tetrahydrocannabinol
cannabidiol
Placebo
Interventions
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tetrahydrocannabinol
cannabidiol
Placebo
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Incidental cannabis use for at least one year, at least four times per year, but less than once a week.
* Dutch-speaking
* Willing to comply with the study procedures
* Having given written informed consent
* Restraint eating (men: score \> 2.90)
* Lack of appetite
* Having difficulties with swallowing/eating
* Usage of an energy restricted diet during the last two months
* Weight loss or weight gain of 5kg or more during the last two months
* Stomach or bowel disease
* Diabetes, thyroid disease, other endocrine disorders
* Use of daily medication except paracetamol
* Having taste or smell disorders (self-report)
* Being allergic/intolerant for products under study
* Previously experienced an adverse reaction to cannabinoids (e.g. anxiety, paranoia, nausea)
* Having (had) a schizophrenia or other psychotic illness
* Having a family history of schizophrenia or other psychotic illness
* Working at the Division of Human Nutrition (WUR)
* Current participation in other research from the Division of Human Nutrition (WUR)
18 Years
35 Years
MALE
Yes
Sponsors
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Wageningen University
OTHER
Responsible Party
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Principal Investigators
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Suzanne EM de Bruijn, MSc
Role: PRINCIPAL_INVESTIGATOR
Wageningen University
Gerry Jager, Dr.
Role: STUDY_CHAIR
Wageningen University
Locations
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Wageningen University
Wageningen, Gelderland, Netherlands
Countries
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Other Identifiers
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2013-002555-14
Identifier Type: EUDRACT_NUMBER
Identifier Source: secondary_id
NL44758.081.13
Identifier Type: -
Identifier Source: org_study_id
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