Strasbourg, Bas-Rhin, 67300, France
NCT Number: NCT01793961
Effects of Chronic Intake of Cannabis on Contrast Sensitivity
Rates of driving under the influence of cannabis have risen in recent years. Cannabis is involved in 1/3 of motor vehicle collisions. The chronic use of cannabis is known to affect dopaminergic regulation and may thus impair contrast sensitivity. In turn, contrast sensitivity disorders could originate difficulties to anticipate and avoid collision with objects, especially when objects are in movement. The investigators goal is to examine the effects of a chronic intake of cannabis on contrast sensitivity. The observed values will be compared to standard references. In addition, since smoking cannabis is always associated with tobacco, the investigators will control the effects of tobacco on contrast sensitivity.
In this study, the investigators will include 36 cannabis addicts, 36 tobacco addicts and 36 no smokers. The investigators will present gratings with different spatial frequencies and the investigators will determine contrast thresholds for static and dynamic (moving) gratings. The investigators predict that cannabis addicts will present abnormal contrast sensitivity especially in case of dynamic presentation of gradings.
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Notify MeKey information
Conditions
Age range
18 year–50 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
"Cannabis" Arm
- patient addicted to cannabis
- Positive CAST test result
- Urine tested positive for cannabis metabolites
"Tobacco" Arm
- positive Fagerström test result
- No cannabis intake in the last year before inclusion
- No previous history of cannabis use
"Healthy Volunteers"
- No tobacco or cannabis intake in the last year before inclusion
- No history of addictive disorders
Exclusion criteria
- addiction to other substances than cannabis or tobacco
- benzodiazepine treatment
- patient with history of benzodiazepine treatment
- patient with history of general anesthesia in the last 3 months before inclusion
- patient with history of head trauma
- Pregnant woman
- breast feeding woman
- Adults under supervision or guardianship
Treatment and study plan
Electroretinogram
Othercontrast sensitivity tests
OtherPrimary outcomes
-
The contrast detection treshold
Time frame: up to 9 days after inclusion
Comparison of the contrast detection threshold of the 3 groups
Sponsors and collaborators
Lead sponsor
University Hospital, Strasbourg, France
Other
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2015
- Study completion
- 2018
- First posted
- Feb 18, 2013
- Registry last updated
- Jun 8, 2026
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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