Assessing Abuse Potential of Parenteral Buprenorphine/Naloxone in Non-Dependent Opioid Abusers
Stopped early · Not applicable
Conditions studied: Opioid-Related Disorders
In brief
Buprenorphine, a treatment for opioid dependence, can be mixed with another drug, naloxone, to limit abuse potential. Parenteral administration (intravenous or intramuscular injection) of buprenorphine/naloxone causes withdrawal symptoms in opioid dependent individuals. However, naloxone does not cause withdrawal symptoms in non-dependent opioid abusers. This study will investigate whether naloxone decreases the opioid agonist effect from injected buprenorphine, hence decreasing the abuse potential of buprenorphine/naloxone, in non-dependent opioid abusers.
Key facts
- Study ID
- NCT00134875
- Run by
- National Institute of Allergy and Infectious Diseases (NIAID)
- People needed
- 9
- Starts
- 2000-12-01
- Expected to finish
- 2017-12-01
- Last updated by the study team
- 2017-01-12
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Non-dependent opioid abuser
- Actively abusing opioids by injection
You may not qualify if…
- Opioid dependence
- Signs or symptoms of opioid withdrawal, once admitted to residential unit
Where it is running
- Johns Hopkins University (BPRU) Bayview Campus — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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