Testing the Interactive Effects of Delta-9-Tetrahydrocannabinol and Pregnenolone: Sub-Study I
- Conditions
- Healthy
- Interventions
- Registration Number
- NCT02811939
- Lead Sponsor
- Yale University
- Brief Summary
The overall purpose of this study is to examine the effect of Pregnenolone (PREG) on the acute psychosis-like and cognitive effects of Delta-9-Tetrahydrocannabinol (THC). This will be tested by pretreating healthy individuals with PREG, and then assessing their responses to Dronabinol (THC).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 13
- Exposed to cannabis at least once in lifetime
- Cannabis naïve
- Individuals with a documented reaction/allergy to Pregnenolone
- Individuals with a documented reaction/allergy to Sesame oil
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Active THC and Placebo Pregnenolone Placebo Pregnenolone - Active THC and Placebo Pregnenolone Active Dronabinol - Active THC and Active Pregnenolone Active Dronabinol - Active THC and Active Pregnenolone Active Pregnenolone - Placebo THC and Active Pregnenolone Active Pregnenolone - Placebo THC and Active Pregnenolone Placebo Dronabinol - Placebo THC and Placebo Pregnenolone Placebo Pregnenolone - Placebo THC and Placebo Pregnenolone Placebo Dronabinol -
- Primary Outcome Measures
Name Time Method Change from Baseline: Positive and Negative Syndrome Scale (PANSS) baseline, 30, 110, 180, and 240 minutes after the administration of oral dronabinol/placebo Positive, negative and general symptoms will be assessed using the positive, negative, and general symptom subscale of the PANSS.
- Secondary Outcome Measures
Name Time Method Change from Baseline: Clinician Administered Dissociative Symptoms Scale (CADSS) baseline, 30, 110, 180, and 240 minutes after the administration of oral dronabinol/placebo Perceptual alterations will be measured using the CADSS. This is a scale consisting of 19 self-reported items, and 9 clinician-rated items. The scale captures alterations in environmental/time/body perception, feelings of unreality, and memory impairment.
Change from Baseline: Psychotomimetic States Inventory (PSI) baseline, 30, 110, 180, and 240 minutes after the administration of oral dronabinol/placebo The PSI is a measure of drug induced psychotomimetic states. This self-reported scale consists of 28 items rated 0 (not at all) to 3 (extremely) and will facilitate the characterization of a wide range of dissociative/hallucinatory phenomena as well as cognitive disorganization associated with the administration of THC.
Change from Baseline: Visual Analog Scale (VAS) Baseline; 30 minutes and 10 minutes prior to administration of oral dronabinol or placebo; 20, 90, 110, 150, 180, and 240 minutes after the administration of oral dronabinol/placebo Feeling states associated with cannabis intoxication will be measured using a self-reported visual analog scale of feeling states associated with cannabis effects (ex. "high, "calm", "anxious"). Subjects will be asked to score the perceived intensity of these feeling states at that moment on a 11mm line. This data will be captured to validate the experiment is relevant to cannabis effect.
Cognitive Test Battery 25 minutes after Dronabinol is given orally Several computer tasks will be administered in order to evaluate the effects of cannabis on verbal learning and memory. The battery consists of five computer tasks that last no longer than 20 minutes in total.
Trial Locations
- Locations (1)
Biological Studies Unit at the VA Connecticut Healthcare System, Yale School of Medicine
🇺🇸West Haven, Connecticut, United States