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Trial NCT00000341

Resource URI: http://static.linkedct.org/resource/trials/NCT00000341
PropertyValue
linkedct:brief_title Evaluation of Liquid vs. Tablet Buprenorphine - 6
linkedct:condition <http://static.linkedct.org/resource/condition/9249>
linkedct:criteria Inclusion Criteria: M/F ages 21-50. Meet DSM-IV criteria for opioid 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.
linkedct:download_date Information obtained from ClinicalTrials.gov on December 30, 2009
linkedct:eligibility_gender Both
linkedct:eligibility_healthy_volunteers No
linkedct:eligibility_maximum_age 50 Years
linkedct:eligibility_minimum_age 21 Years
linkedct:end_date August 2000
linkedct:enrollment 1 (xsd:int)
linkedct:firstreceived_date September 20, 1999
linkedct:id NCT00000341
rdfs:label Trial NCT00000341
linkedct:lastchanged_date August 26, 2008
linkedct:lead_sponsor_agency National Institute on Drug Abuse (NIDA)
linkedct:location <http://static.linkedct.org/resource/location/209856>
linkedct:nct_id NCT00000341
linkedct:number_of_arms 0 (xsd:int)
linkedct:number_of_groups 0 (xsd:int)
linkedct:official_title Pharmacokinetics and Bioavailability of Liquid vs Tablet Buprenorphine
linkedct:org_study_id NIDA-3-0010-6
linkedct:overall_official <http://static.linkedct.org/resource/overall_official/60742>
linkedct:overall_status Completed
linkedct:oversight <http://static.linkedct.org/resource/oversight/2918>
foaf:page <http://clinicaltrials.gov/show/NCT00000341>
linkedct:phase Phase 2
linkedct:primary_outcomes <http://static.linkedct.org/resource/primary_outcomes/20855>
linkedct:secondary_id Y01-3-0010-6
linkedct:source National Institute on Drug Abuse (NIDA)
linkedct:start_date August 1996
linkedct:study_design Treatment, Randomized, Double-Blind, Crossover Assignment
linkedct:study_type Interventional
linkedct:summary The purpose of this study is to evaluate the steady-state pharmacokinetics and bioavailability of buprenorphine sublingual tablets vs. sublingual solution.
rdf:type linkedct:trials
linkedct:verification_date August 2008