Evaluation of Lofexidine for Treatment of Opiate Withdrawal - 10
Completed · Phase 1
Conditions studied: Opioid-Related Disorders
In brief
The purpose of this study is to assess the safety of lofexidine in the treatment of opiate-dependent individuals.
Key facts
- Study ID
- NCT00000345
- Run by
- National Institute on Drug Abuse (NIDA)
- People needed
- 0
- Starts
- 1996-04-01
- Last updated by the study team
- 2017-01-12
Who can join
Age: 21 and older, up to 50. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- M/F ages 21-50. Meet DSM-IV criteria for opiate dependence. Agree to conditions of the study and sign informed consent.
You may not qualify if…
- 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.
Where it is running
- Friends Research Institute — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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