Effects of Labetalol on Human Cocaine Use - 8
2 other identifiers
interventional
N/A
1 country
1
Brief Summary
The purpose of this study is to determine the effect of labetalol treatment on the subjective and physiological effects of cocaine.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Oct 1997
Typical duration for phase_2
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 1997
CompletedFirst Submitted
Initial submission to the registry
September 20, 1999
CompletedFirst Posted
Study publicly available on registry
September 21, 1999
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2001
CompletedJanuary 12, 2017
November 1, 2016
September 20, 1999
January 11, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Subjective
Physiological measures
Interventions
Eligibility Criteria
You may qualify if:
- Male/Female ages 20-55. History of smoked or intravenous cocaine use on the average of at least once a week over a six month period. Current history of good health and normal EKG. Not pregnant as determined by pregnancy screening nor breat feeding and using acceptable birth control methods (e.g. birth control pills diaphragm, condoms, plus foam) during the study.
You may not qualify if:
- Current problems with major psychiatric illnesses including bipolar disorder, schizophrenia, or anxiety disorders. Current dependence on alcohol or on durgs other than cocaine. History of major medical illnesses including asthma and chronic obstructive pulmonary disease. Currently on a drug related parole or probation. Treated for chemical dependency within the past 6 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- National Institute on Drug Abuse (NIDA)lead
- University of Minnesotacollaborator
Study Sites (1)
University of Minnesota
Minneapolis, Minnesota, 55455, United States
Related Publications (1)
Pharmacol. Biochem. Behav (accepted). None
BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Dorothy Hatsukami, Ph.D.
University of Minnesota
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Masking
- DOUBLE
- Purpose
- TREATMENT
- Sponsor Type
- NIH
Study Record Dates
First Submitted
September 20, 1999
First Posted
September 21, 1999
Study Start
October 1, 1997
Study Completion
December 1, 2001
Last Updated
January 12, 2017
Record last verified: 2016-11