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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00893269
Other study ID # NA_00017909
Secondary ID R21DA025794
Status Completed
Phase Phase 1
First received April 30, 2009
Last updated December 3, 2013
Start date October 2008
Est. completion date October 2010

Study information

Verified date December 2013
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Heavy marijuana users report experiencing trouble sleeping when they try to quit, but this has not been carefully studied. This research is being done to learn more about sleep function in heavy marijuana users, and to determine whether a medication approved for treating insomnia can help restore normal sleep function during brief periods of abstinence.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date October 2010
Est. primary completion date October 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- current use of marijuana

- able to give informed consent

Exclusion Criteria:

- dependence on drug other than marijuana

- current sleep disorder

- pregnant, breast feeding, or planning to become pregnant within the next 3 months

- currently seeking treatment for cannabis-related problems or otherwise trying to reduce use

- use of cannabis under the guidance of a physician for a medical disorder

- unstable or uncontrolled cardiovascular disease (e.g., hypertension, angina)

- allergy to study medication

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
eszopiclone
Oral capsule at dose recommended for adults
Placebo
Participants receive placebo prior to sleep
ramelteon
ramelteon
zolpidem
zolpidem

Locations

Country Name City State
United States Johns Hopkins University Baltimore Maryland

Sponsors (3)

Lead Sponsor Collaborator
Johns Hopkins University Food and Drug Administration (FDA), National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Marijuana Withdrawal Every day during study participation No
Secondary Objective Sleep Assessment Every day during study participation No
Secondary Cognitive Performance Every day during study participation No
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