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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02291562
Other study ID # LOGIN_EpMem
Secondary ID
Status Completed
Phase N/A
First received November 11, 2014
Last updated January 15, 2015
Start date July 2014
Est. completion date December 2014

Study information

Verified date November 2014
Source Central Institute of Mental Health, Mannheim
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

THC and CBD have distinct symptomatic and behavioral effects. In healthy individuals, THC can induce psychotic symptoms and anxiety, and can impair memory. In contrast, CBD has anxiolytic and possibly antipsychotic properties, while not impairing memory and other cognitive functions. Instead, CBD has been shown to have significant neuroprotective effects. In humans, CBD values correlated positively with gray matter concentration in bilateral hippocampus. Recent data from experimental animals and in vitro studies suggest that these distinct effects might be caused by opposing effects on brain cannabinoid receptors.

Neuroimaging studies have consistently identified brain activity recorded at prefrontal and medial temporal regions as relevant for episodic memory. Additionally, the abundance of cannabinoid receptors in the hippocampus and the parahippocampal and entorhinal cortices suggests a potential impact of CBD in memory deficits typical in healthy aging. However, the evidence relating cannabinoids to these conditions is relatively recent and has been obtained from either biochemical or pharmacological studies. It might be hypothesized that CBDs could be useful to delay or even arrest the progression of functional and structural neuronal degeneration.

The investigators will use an episodic memory paradigm to test the effects of THC, CBD and placebo on memory encoding and retention and the underlying neuronal networks on healthy male subjects.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- no acute or chronic disease

Exclusion Criteria:

- opioid intake

- medication or drug abuse

- kidney or liver dysfunction

- claustrophobia

- none removable metallic parts (e.g. hip replacement)

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
Tetrahydrocannabinol
10 mg Tetrahydrocannabinol (capsule, once) oral intake
Cannabidiol
600 mg Cannabidiol (capsule, once) oral intake
placebo
placebo (capsule, once) oral intake

Locations

Country Name City State
Germany Central Institute of Mental Health Mannheim

Sponsors (1)

Lead Sponsor Collaborator
Central Institute of Mental Health, Mannheim

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in BOLD (blood oxygen level dependent) responses Differential changes of the BOLD response under the three different conditions (THC, CBD, placebo) during the learning and the test phase of the memory paradigm immediate No
Secondary Changes in behavioral measures Differential changes in reaction times and number of correct responses during the three different conditions (THC, CBD, placebo) immediate No
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