Pharmacokinetic and Pharmacodynamic Effects of Smoked and Vaporized Cannabis

NCT ID: NCT03676166

Last Updated: 2019-09-13

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-06-16

Study Completion Date

2017-01-17

Brief Summary

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Few studies have been conducted to assess the pharmacokinetic and pharmacodynamic effects of smoked and vaporized cannabis. Careful analysis of different cannabis administration methods on these parameters is required to determine the level and duration of biological cannabinoid exposure and associated subjective, cardiovascular and cognitive effects. In the present study the investigators evaluated the detection of cannabinoids in whole blood, oral fluid, and urine, as well as the acute pharmacodynamics associated with smoked and vaporized cannabis among individuals who were not regular cannabis users. The outcomes of the study will extend scientific knowledge about the behavioral pharmacology and toxicology of smoked and vaporized cannabis administration and can inform policies regarding clinical, workplace and roadside drug testing programs.

Detailed Description

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Conditions

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Cannabis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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0mg THC smoked cannabis

placebo smoked cannabis

Group Type EXPERIMENTAL

Cannabis

Intervention Type DRUG

Inhaled cannabis

10mg THC smoked cannabis

smoked cannabis containing 10mg THC

Group Type EXPERIMENTAL

Cannabis

Intervention Type DRUG

Inhaled cannabis

25mg THC smoked cannabis

smoked cannabis containing 25mg THC

Group Type EXPERIMENTAL

Cannabis

Intervention Type DRUG

Inhaled cannabis

0mg THC vaporized cannabis

placebo vaporized cannabis

Group Type EXPERIMENTAL

Cannabis

Intervention Type DRUG

Inhaled cannabis

10mg THC vaporized cannabis

vaporized cannabis containing 10mg THC

Group Type EXPERIMENTAL

Cannabis

Intervention Type DRUG

Inhaled cannabis

25mg THC vaporized cannabis

vaporized cannabis containing 25mg THC

Group Type EXPERIMENTAL

Cannabis

Intervention Type DRUG

Inhaled cannabis

Interventions

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Cannabis

Inhaled cannabis

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Have provided written informed consent
2. Be between the ages of 18 and 45
3. Be in good general health based on a physical examination, medical history, vital signs, 12-lead ECG and screening urine and blood tests
4. Test negative for recent cannabis use in urine at the screening visit (confirmed by GC/MS laboratory test) and at clinic admission
5. Test negative for other drugs of abuse, including alcohol at the screening visit and at clinic admission
6. Not be pregnant or nursing (if female). All females must have a negative serum pregnancy test at the screening visit and a negative urine pregnancy test at clinic admission.
7. Have a body mass index (BMI) in the range of 19 to 36 kg/m2
8. Blood pressure at Screening Visit does not exceed a systolic blood pressure (SBP) of 150 mmHg or a diastolic blood pressure (DBP) of 90 mmHg

Exclusion Criteria

1. Non-medical use of psychoactive drugs other than, nicotine, alcohol, or caffeine 3 month prior to the Screening Visit;
2. History of or current evidence of significant medical or psychiatric illness judged by the investigator to put the participant at greater risk of experiencing an adverse event due to exposure or completion of other study procedures.
3. Use of an OTC, systemic or topical drug(s), herbal supplement(s), or vitamin(s) within 14 days of experimental sessions; which, in the opinion of the investigator or sponsor, will interfere with the study result or the safety of the subject.
4. Use of a prescription medication (with the exception of birth control prescriptions) within 14 days of experimental sessions; which, in the opinion of the investigator or sponsor, will interfere with the study result or the safety of the subject.
5. Use of hemp seeds or hemp oil in any form in the past 3 months.
6. Use of dronabinol (Marinol) within the past 6 months.
7. History of xerostomia (dry mouth), or the presence of mucositis, gum infection or bleeding, or other significant oral cavity disease or disorder that in the investigator's opinion may affect the collection of oral fluid samples.
8. History of clinically significant cardiac arrhythmias or vasospastic disease (e.g., Prinzmetal's angina).
9. Abnormal EKG result that in the investigator's opinion is clinically significant.
10. Enrolled in another clinical trial or have received any drug as part of a research study within 30 days prior to dosing.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Johns Hopkins University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ryan Vandrey, PhD

Role: PRINCIPAL_INVESTIGATOR

Johns Hopkins School of Medicine Behavioral Pharmacology Research Unit

Locations

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Johns Hopkins School of Medicine Behavioral Pharmacology Research Unit

Baltimore, Maryland, United States

Site Status

Countries

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United States

References

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Spindle TR, Cone EJ, Schlienz NJ, Mitchell JM, Bigelow GE, Flegel R, Hayes E, Vandrey R. Acute Effects of Smoked and Vaporized Cannabis in Healthy Adults Who Infrequently Use Cannabis: A Crossover Trial. JAMA Netw Open. 2018 Nov 2;1(7):e184841. doi: 10.1001/jamanetworkopen.2018.4841.

Reference Type DERIVED
PMID: 30646391 (View on PubMed)

Other Identifiers

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IRB_00035394

Identifier Type: -

Identifier Source: org_study_id

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