Depot Naltrexone Mechanism of Action in Heroin Dependent Patients Using fMRI and SPECT (XRNT)
Primary Purpose
Opioid-Related Disorders, Heroin Dependence
Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Naltrexone
Sponsored by
About this trial
This is an interventional basic science trial for Opioid-Related Disorders focused on measuring opioid dependence, heroin dependence, extended release depot naltrexone, functional Magnetic Resonance Imaging, dopamine transporter, Single Photon Emission Computed Tomography
Eligibility Criteria
Inclusion Criteria:
- Heroin dependent patients: have a diagnosis of opioid dependence according to DSM-IV criteria, heroin as primary drug of abuse and inhalation as primary route of administration.
- Healthy controls: no diagnosis of substance dependence, no current psychotropic medication. Care will be taken to match controls for gender, age, smoking status, IQ and handedness.
Exclusion Criteria:
- Age below 18 or over 55
- Medical contraindications for XRNT or MRI (Langleben 2006; Langleben, Ruparel et al. 2008). Briefly, the former include candidates with known hypersensitivity to naltrexone,PLG (poly-lactide-coglycolide), carboxymethylcellulose, or any other components of the Vivitrol® diluent, hepatic or renal disease, chronic pain syndromes, female subjects who are pregnant or lactating, or are of child bearing potential and are not using an acceptable method of birth control. MRI contraindications include chronic medical (neurological, cardiovascular, infectious, metabolic, etc) conditions that may affect the brain morphology and/or activity and indwelling foreign metallic or magnetically sensitive objects and devices, such as shrapnel, pacemakers, orthopaedic fixation devices or vascular stents
- Presence of disorders precluding normal perception of visual and auditory stimuli, such as color blindness, deafness, severe myopia, etc.
- Patients with a history of or current psychosis or current major depressive disorder with suicidal ideation
- Patients who are being treated under forced treatment conditions
- History or evidence of disorders that may affect cerebral function or circulation, such as diabetes and other metabolic disorders, encephalopathy, cardiovascular or cerebrovascular disease, history of head trauma with depressed skull fracture or prolonged loss of consciousness and history of brain surgery
- Female subjects: women who are pregnant or breast-feeding
- Current psychotropic medication
- Use of any prescription medications that could affect alertness or the circulatory system
- IQ < 70
- Naltrexone use within the past 6 months
- Baseline aspartate aminotransferase or alanine aminotransferase more than three times the upper limit of normal
- Patients with no intention to be opioid-free for a minimum of 7 days before starting XRNT treatment
Sites / Locations
- Academic Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Depot Naltrexone
Arm Description
Outcomes
Primary Outcome Measures
Brain functions
Brain functions of 20 heroin addicts just before and during a three month extended release naltrexone treatment using both functional MRI and dopamine transporter SPECT, compared to brain functions of 20 healthy controls.
Secondary Outcome Measures
Feasibility and potential efficacy
The feasibility and potential efficacy of extended release naltrexone in a pilot sample of 20 Dutch heroin addicts in terms of (a) the percentage of patients that actually starts treatment when invited and (b) the percentage of 3 months retention.
Full Information
NCT ID
NCT01471145
First Posted
November 10, 2011
Last Updated
October 10, 2014
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development, Alkermes, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT01471145
Brief Title
Depot Naltrexone Mechanism of Action in Heroin Dependent Patients Using fMRI and SPECT
Acronym
XRNT
Official Title
Feasibility, Mechanism of Action and Potential Side Effects of Extended Release Depot Naltrexone in Opioid Dependent Patients
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development, Alkermes, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this project is to study brain functions of 20 heroin addicts (compared to brain functions of 20 healthy controls) just before and during a three month extended release naltrexone treatment using functional MRI and dopamine transporter SPECT.
The following hypotheses are tested:
XRNT modulates the fMRI response to drug cues in predetermined brain regions.
The expression of striatal transporters (assessed with SPECT) will decrease after a three-month course of extended release naltrexone
Detailed Description
Heroin dependence is a quintessential international health problem, with a significant prevalence. Drug free treatments, including pharmacologically supported interventions using oral naltrexone, have not been very successful, mainly due to low compliance. The recent introduction of Vivitrol®, consisting of monthly injections, may create new opportunities. Vivitrol® is an innovative treatment delivery method that blocks the rewarding effects of heroin.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid-Related Disorders, Heroin Dependence
Keywords
opioid dependence, heroin dependence, extended release depot naltrexone, functional Magnetic Resonance Imaging, dopamine transporter, Single Photon Emission Computed Tomography
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Depot Naltrexone
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Naltrexone
Other Intervention Name(s)
Vivitrol
Intervention Description
naltrexone for extended-release injectable suspension, 380 mg/vial, every 4 weeks or once a month
Primary Outcome Measure Information:
Title
Brain functions
Description
Brain functions of 20 heroin addicts just before and during a three month extended release naltrexone treatment using both functional MRI and dopamine transporter SPECT, compared to brain functions of 20 healthy controls.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Feasibility and potential efficacy
Description
The feasibility and potential efficacy of extended release naltrexone in a pilot sample of 20 Dutch heroin addicts in terms of (a) the percentage of patients that actually starts treatment when invited and (b) the percentage of 3 months retention.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Heroin dependent patients: have a diagnosis of opioid dependence according to DSM-IV criteria, heroin as primary drug of abuse and inhalation as primary route of administration.
Healthy controls: no diagnosis of substance dependence, no current psychotropic medication. Care will be taken to match controls for gender, age, smoking status, IQ and handedness.
Exclusion Criteria:
Age below 18 or over 55
Medical contraindications for XRNT or MRI (Langleben 2006; Langleben, Ruparel et al. 2008). Briefly, the former include candidates with known hypersensitivity to naltrexone,PLG (poly-lactide-coglycolide), carboxymethylcellulose, or any other components of the Vivitrol® diluent, hepatic or renal disease, chronic pain syndromes, female subjects who are pregnant or lactating, or are of child bearing potential and are not using an acceptable method of birth control. MRI contraindications include chronic medical (neurological, cardiovascular, infectious, metabolic, etc) conditions that may affect the brain morphology and/or activity and indwelling foreign metallic or magnetically sensitive objects and devices, such as shrapnel, pacemakers, orthopaedic fixation devices or vascular stents
Presence of disorders precluding normal perception of visual and auditory stimuli, such as color blindness, deafness, severe myopia, etc.
Patients with a history of or current psychosis or current major depressive disorder with suicidal ideation
Patients who are being treated under forced treatment conditions
History or evidence of disorders that may affect cerebral function or circulation, such as diabetes and other metabolic disorders, encephalopathy, cardiovascular or cerebrovascular disease, history of head trauma with depressed skull fracture or prolonged loss of consciousness and history of brain surgery
Female subjects: women who are pregnant or breast-feeding
Current psychotropic medication
Use of any prescription medications that could affect alertness or the circulatory system
IQ < 70
Naltrexone use within the past 6 months
Baseline aspartate aminotransferase or alanine aminotransferase more than three times the upper limit of normal
Patients with no intention to be opioid-free for a minimum of 7 days before starting XRNT treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wim van den Brink, MD PhD
Organizational Affiliation
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Academic Medical Center
City
Amsterdam
ZIP/Postal Code
P.O. Box 22660
Country
Netherlands
12. IPD Sharing Statement
Citations:
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9437624
Citation
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Depot Naltrexone Mechanism of Action in Heroin Dependent Patients Using fMRI and SPECT
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