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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01394185
Other study ID # NA_00041251
Secondary ID R01DA025044
Status Completed
Phase Phase 1/Phase 2
First received July 12, 2011
Last updated August 2, 2017
Start date February 2011
Est. completion date September 2012

Study information

Verified date August 2017
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study participants received dronabinol (0, 120mg/day and 240mg/day) for 12 consecutive days in a randomized order. During each dronabinol maintenance period they were able to self-administer active or placebo cannabis using either a progressive ratio schedule or choice between cannabis and monetary alternative.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date September 2012
Est. primary completion date September 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- Current use of marijuana

- Able to give informed consent

Exclusion Criteria:

- Daily use of psychoactive medication

- Current Axis I psychiatric disorder other than dependence on cannabis or nicotine, or abuse of drugs or alcohol

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

- Those seeking treatment for cannabis-related problems or using cannabis under the guidance of a physician for a medical disorder

- Uncontrolled or unstable cardiovascular disease

- Allergy to sesame oil

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dronabinol 120mg/day
Participants receive 40mg dronabinol 3 times daily
Placebo
Participants receive placebo
Dronabinol 240mg/day
Participants receive 80mg dronabinol 3 times daily

Locations

Country Name City State
United States Johns Hopkins University (Bayview Campus) Baltimore Maryland

Sponsors (2)

Lead Sponsor Collaborator
Johns Hopkins University National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Marijuana Self-administration - Progressive Ratio Participants will be able to self-administer cannabis cigarettes (weighing about 0.8 grams and with about 6% THC) under a progressive ratio schedule. The number of progressive ratios completed (and thus, cannabis cigarettes consumed) is the primary study endpoint 12-day Dronabinol maintenance period
Primary Marijuana Self-administration - Drug Vs Money Choice Participants will be able to self-administer cannabis cigarettes (weighing about 0.8 grams and with about 6% THC) in 5 discrete choices each day between one cannabis cigarette and $1. The number of cannabis cigarettes chosen (and subsequently self-administered) is the primary study endpoint 12-day Dronabinol maintenance period
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