Phase 3
N=8
Vaping THC From Electronic Cigarettes
Marijuana Dependence
Bottom Line
View on ClinicalTrials.gov: NCT02955329 ↗Enrolled (actual)
8
Serious AEs
0.0%
Results posted
Apr 2021
Primary outcome: Primary: Mean Delivered and Retained Doses — 0.016; 0.018; 0.026 grams (g)
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 3
- Interventions
- Nicotine (Drug); Cannabis (Drug); PAX Loose Leaf Vaporizer (Device)
- Age
- Adult, Older Adult · 21+ yrs
- Sex
- All
- Sponsor
- University of California, San Francisco
- Primary completion
- Nov 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean Delivered and Retained Doses |
0.016; 0.018; 0.026 | — |
| PRIMARY Median Peak THC Concentration (Cmax) |
1.52; 9.72; 25.74 | — |
| PRIMARY Median Peak Nicotine Concentration (Cmax) |
0.55; 0.38; 1.59 | — |
| PRIMARY Median THC Exposure |
201.6; 306.4; 585.6 | — |
| PRIMARY Median Nicotine Exposure |
63.1; 42.7; 134.9 | — |
| PRIMARY Mean Heart Rate |
67.3; 66.8; 70.5 | — |
| PRIMARY Mean Score on the Drug Effects Questionnaire (DEQ) |
45.4; 69.0; 73.2 | — |
| PRIMARY Mean Scores on the Marijuana Craving Questionnaire-Short Form (MCQ-SF) |
2.8; 3.0; 2.5; 3.1; 3.5; 2.9 | — |
| PRIMARY Mean Scores on the Modified Cigarette Evaluation Questionnaire (mCEQ) |
1.5; 3.1; 1.4 | — |
| PRIMARY Mean Scores on the Positive Affect Negative Affect Schedule (PANAS) |
26.9; 23.0; 25.8; 10.6; 11.4; 10.2 | — |
| PRIMARY Mean Scores on the Minnesota Nicotine Withdrawal Scale (MNWS) |
0.8; 1.2; 0.9 | — |
Summary
This study aims to understand THC pharmacology and the safety of cannabis vaping, including the pharmacology and safety of co-administration of nicotine and THC. The study is designed as a within-subjects single-blinded crossover study. Fourteen smokers of tobacco cigarettes and cannabis will switch between three conditions, namely: (a) vaping cannabis leaf, (b) vaping tobacco containing nicotine and (c) vaping a combination of cannabis leaf and tobacco containing nicotine. All participants will vape each product with the PAX loose-leaf vaporizer. The study will be conducted during three outpatient visits separated by at least 48 hours. The order of treatment (cannabis leaf, tobacco with nicotine, cannabis leaf & tobacco with nicotine) will be counterbalanced between subjects. Subjects will be blinded to the content of the vaporizer on the study day but will be told during screening that they will vape cannabis alone, tobacco alone, and cannabis plus tobacco with nicotine.
Eligibility Criteria
Inclusion
- Age >=21 years 90 (considered out of range if both machine and manual readings are above/below these thresholds)
- Diastolic Blood Pressure 50 (considered out of range if both machine and manual readings are above/below these thresholds)
- Body Mass Index ≤<=38.0
Exclusion
- Medical (The following unstable medical conditions):
- Heart disease
- Uncontrolled hypertension
- Thyroid disease (okay if controlled with medication)
- Diabetes
- Hepatitis B or C or Liver disease
- Glaucoma
- Prostatic hypertrophy
- History of paranoia after marijuana use
- Psychiatric conditions
- Current or past schizophrenia, and/or current or past bipolar disorder
- Adult onset Attention-deficit/hyperactivity disorder (ADHD) (if being treated)
- Participants with current or past depression and/or anxiety disorders will be reviewed by the study physician and considered for inclusion
- History of psychiatric hospitalizations are not exclusionary, but study participation will be determined as per study physician's approval
- Drug/Alcohol Dependence
- Alcohol or illicit drug dependence within the past 12 months with the exception of those who have recently completed an alcohol/drug treatment program and are currently abstaining from drug and alcohol
- Positive toxicology test at the screening visit (THC & prescribed medications okay)
- Methadone replacement therapy
- Scoring a 2 or higher on the Severity of Dependence Scale for cannabis use.
- Psychiatric medications
- Current regular use of any psychiatric medications with the exception of Selective Serotonin Reuptake Inhibitors (SSRIs) and serotonin-norepinephrine reuptake Inhibitors (SNRIs) and current evaluation by the study physician that the participant is otherwise healthy, stable, and able to participate.
- Other Medications
- Use of medications that are inducers of nicotine metabolizing enzyme CYP2A6 (Example: rifampicin, dexamethasone, phenobarbital, and other anticonvulsant drugs).
- Concurrent use of nicotine-containing medications
- Other/Misc. Chronic Health Conditions
- Oral thrush
- Fainting
- Untreated thyroid disease
- Other "life threatening illnesses" as per study physician's discretion
- Use of Other Tobacco Products (OTP); any of the following products in combination more than 15 times in the past month
- smokeless tobacco
- pipes
- cigars, cigarillos
- blunts, spliffs
- Pregnancy
- Pregnancy (self-reported and urine pregnancy test)
- Breastfeeding (determined by self-report)
- Concurrent participation in another clinical trial
- Inability to communicate in English
- Planning to quit smoking or cannabis use within the next 60 days
Data sourced from ClinicalTrials.gov (NCT02955329). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.