Opiate Dependence: Combined Naltrexone/Behavior Therapy - 1
NCT ID: NCT00238914
Last Updated: 2012-01-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE2
12 participants
INTERVENTIONAL
1999-08-31
2002-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
1. Outpatient treatment with Behavioral Naltrexone Therapy will yield a lower rate of relapse to illicit opiates compared to naltrexone plus Compliance Enhancement (CE) Therapy.
2. Lifetime history of depression will predict dysphoria and non-compliance with naltrexone.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Behavioral Naltrexone Therapy: A Novel Treatment for Heroin Dependence
NCT00332228
Behavioral Naltrexone Therapy for Promoting Adherence to Oral Naltrexone vs Extended Release Injectable Depot Naltrexone
NCT00577408
Depot Naltrexone Treatment of Opioid Dependent Parolees
NCT00756990
Buprenorphine/Naloxone Stabilization and Induction Onto Injection Naltrexone
NCT02294253
Dronabinol Naltrexone Treatment for Opioid Dependence
NCT01024335
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
CE plus oral naltrexone
Compliance enhancement plus oral naltrexone
Naltrexone
50mg of oral naltrexone daily
Compliance Enhancement (CE)
a controlled therapy intended to simulate outpatient psychiatric care.
BNT plus oral naltrexone
Behavioral naltrexone therapy plus oral naltrexone
Naltrexone
50mg of oral naltrexone daily
Behavioral Naltrexone Therapy (BNT)
a hybrid of Relapse Prevention, the Community Reinforcement Approach, and Network Therapy
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Naltrexone
50mg of oral naltrexone daily
Behavioral Naltrexone Therapy (BNT)
a hybrid of Relapse Prevention, the Community Reinforcement Approach, and Network Therapy
Compliance Enhancement (CE)
a controlled therapy intended to simulate outpatient psychiatric care.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Meets DSM-IV criteria for current opiate dependence disorder of at least six months duration, supported by a positive urine for opiates and further by a positive naloxone challenge test if the diagnosis is unclear.
3. Able to give informed consent.
4. At least one significant other is willing to be interviewed for possible participation in the treatment.
Exclusion:
1. Pregnancy, lactation, or failure in a sexually active woman to use adequate contraceptive methods.
2. Active medical illness which might make participation hazardous, such as untreated hypertension, unstable cardiovascular disease, acute hepatitis with SGOT or SGPT \> 2-3 times normal, unstable diabetes, AIDS dementia.
3. Active psychiatric disorder which might interfere with participation or make participation hazardous, including DSM-IV schizophrenia, bipolar disorder with mania or psychosis, and depressive disorder with suicide risk of 1 or more suicide attempts within the past year.
4. History of allergic reaction to naloxone, naltrexone, buprenorphine, clonidine, or clonazepam.
5. Currently prescribed or regularly taking opiates for chronic pain or medical illness.
6. Current participation in another intensive treatment program or currently prescribed psychotropic medications in the last 30 days.
7. Current participation in a Methadone Maintenance program and/or regular and/or Dependent use of street methadone.
8. Opiate-dependent individuals who are seeking methadone maintenance treatment.
9. History of accidental drug overdose in the last three years as defined as an episode of opioid-induced unconsciousness or incapacitation, whether or not medical treatment was sought or received.
18 Years
60 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Institute on Drug Abuse (NIDA)
NIH
New York State Psychiatric Institute
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Edward Nunes, M.D.
Role: PRINCIPAL_INVESTIGATOR
New York State Psychiatric Institute
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
New York State Psychiatric Institute
New York, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Related Info
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
R01-10746-1
Identifier Type: -
Identifier Source: secondary_id
#4260R
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.