New York State Psychiatric Institute
New York, 10032, United States
NCT Number: NCT00373503
The purpose of this study is to investigate the interaction between marijuana and two potential treatment medications: lofexidine and oral THC, with the direct goal of using this information to improve marijuana treatment outcome.
Looking for future studies?
Notify Me21 year–45 year
All sexes
Interventional
Phase 2
New York, 10032, United States
Only a small percentage of dependent-marijuana smokers who are seeking treatment for their marijuana use is able to achieve sustained abstinence. The objective of this study is to investigate the interaction between marijuana and two potential treatment medications: lofexidine and oral THC, with the direct goal of using this information to improve marijuana treatment outcome. In mice, the α2-receptor agonist, clonidine, reversed symptoms of cannabinoid withdrawal (Lichtman et al., 2001). The purpose of this study is to determine if lofexidine, an α2-receptor agonist with a more favorable side-effect profile than clonidine, decreases symptoms of marijuana withdrawal and thus decreases marijuana relapse, as compared to placebo. Oral THC is FDA-approved for appetite enhancement. Lofexidine, which is currently not FDA-approved, is used in Europe to treat symptoms of heroin withdrawal, and to treat hypertension. For the purposes of this model, relapse is defined to a return to marijuana use after a period of abstinence. We have shown that oral THC reduces symptoms of marijuana withdrawal at doses that produce minimal intoxication (Haney et al., 2004). Thus, the effects of oral THC alone and in combination with lofexidine will be determined. The study will utilize an inpatient/outpatient, counter-balanced design, with each participant maintained on each of four medication conditions for 8 days each: placebo, lofexidine, oral THC, and oral THC combined with lofexidine. During the inpatient study phases, participants will have the opportunity to self-administer placebo or active marijuana 6 times per day. Outpatient phases are for medication clearance so no medications will be administered. This study will provide important information of the effect of these potential treatment medications on both marijuana withdrawal symptoms, and on subsequent marijuana self-administration.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
alpha 2 adrenergic agonist, hypothesized to decrease noradrenergic activity
Other names: Britlofex
cannabinoid agonist hypothesized to decrease MJ withdrawal
Other names: THC
marijuana intoxication, withdrawal and relapse assessed
Other names: cannabis
Time frame: 4 days
Time frame: 3 days
Time frame: 7 days
New York State Psychiatric Institute
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04965012
Behavior, Chemically-Induced Disorders
Winnipeg, Manitoba, Canada
View Trial DetailsNCT02955329
Behavior, Chemically-Induced Disorders
San Francisco, California, United States
View Trial DetailsNCT02579421
Chemically-Induced Disorders, Marijuana Abuse
Minneapolis, Minnesota, United States
View Trial DetailsNCT00480441
Behavior, Behavior, Addictive
Philadelphia, Pennsylvania, United States
View Trial Details