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Infusion Laboratory: Protocol 2 (Lisuride) - 3

Phase 1
Conditions
Cocaine-Related Disorders
Registration Number
NCT00000338
Lead Sponsor
National Institute on Drug Abuse (NIDA)
Brief Summary

The purpose of this study is to evaluate clinical safety issues pertaining to lisuride, to cocaine, and to its interaction in a chronic, crack dependent population, and to determine how pretreatment with lisuride modifies the subjective as well as physiological effects of cocaine.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
2
Inclusion Criteria

M/F ages 21-50. Meet DSM-IV criteria for cocaine dependence. Agree to conditions of the study and sign informed consent.

Exclusion Criteria

Psychiatric disorder that requires medication therapy. History of seizures. Pregnant and/or nuring women. Dependence on ETOH or benzodiazepines or other sedative/hypnotics. Acute hepatitis. Other medical condtions that deem participation to be unsafe.

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evidence of change in neurophysiology and brain ac
Clinical physiological response to cocaine challen
Characterization of study population
Degree of drug craving
History, incidence and amount of drug use
Type and severity of stimulant withdrawal symptoms
Evidence of change in subjective responses to coca
Frequency and intensity of drug use and sexual beh
Degree to which study medication influences change
Population incidence of symptoms of depression, po
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Friends Research Institute

🇺🇸

Los Angeles, California, United States

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