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Effects of different forms of vaporized Cannabis sativa L. *Afina* in cannabis users

Effects of different forms of vaporized Cannabis sativa L. *Afina* in cannabis users - Effects of vaporized cannabis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON50058
Enrollment
25
Registered
2020-06-29
Start date
2021-04-12
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

no health condition is addressed in the research, and healthy volunteers who are occasional cannabis users will be recruited n.a.

Interventions

Participants will undergo 4 experimental conditions, in which they receive a fixed dose of Bedrocan cannabis in different forms (granulate, powder and yellowcake) or placebo. In each condition, the

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Occasional cannabis users (>10 lifetime exposures and

Exclusion criteria

Exclusion criteria: • History of drug abuse (other than the use of cannabis) or addiction (determined by the medical questionnaire, drug questionnaire and medical examination) • Pregnancy or lactation (pregnancy test, if needed) • Hypertension (diastolic > 90; systolic > 140) • Current or history of psychiatric disorder (determined by the medical questionnaire and medical examination) • Liver dysfunction • Any serious prior adverse response to cannabis • History of cardiac dysfunctions (e.g. arrhythmia, ischemic heart disease)

Design outcomes

Primary

MeasureTime frame
The inhalation process and the overall satisfaction with the use of the IMPs will be assessed by the means of Likert scales.

Secondary

MeasureTime frame
Subjective drug effects will be measured by a series of VAS/Bowdle questionnaire/CADDS. The assessment of the quality of the IMPs by participants will be measured by a series of Likert scales. Cognition will be assessed by a computerized test battery. Memory, i.e. sensitivity to go along with suggested self-incriminating statements will be assessed using an adjusted false confession paradigm.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)