- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01668706
Pharmacogenomics Study of Sleep Disturbance and Neurocognitive Impairments in the Opioid Addicts
Opioid abuse is a complex problem, which not only impacts on addicts' physical and psychological health individually, but also threats the society. Recently, spread of HIV via sexual behavior and needle sharing among injecting drug users (IDUs) also becomes a serious public health problem all over the world. In Taiwan, since the first HIV-infected IDU identified in 1987, the incident cases have mounted to 2,461 in 2005. To prevent the epidemics of HIV among IDUs, the Center for Disease Control (CDC) thus collaborated with Department of Justice and implemented harm reduction programs in 2005. It is the milestone that opioid addiction is officially treated as a health rather than a legal issue in Taiwan. Among the harm reduction programs of needle and syringe exchange for IDUs as well as substitution treatment for opioid dependence, methadone maintenance treatment (MMT) is one of the most important parts. Till 2008, there were over 13,000 heroin addicts participated in more than 80 MMT programs.
Although the clinical evidences have proven the superior effectiveness of maintenance therapy in ameliorating illicit substances abuse, decreasing criminality and improving quality of life, there are common problems of sleep disturbance and neurocognitive impairments among the subjects receiving opioid medications. The concerns of the adverse effects might thus frustrate the subjects' motivation and compliance to maintain treatments. However, sleep disturbance and neurocognitive impairments related to opioid medications are often neglected in the clinical practices and there are scanty researches focusing on these crucial issues in the existing literature.
In this prospective study, four groups of subjects including methadone maintenance treatment, buprenorphine/naloxone, medication-free opioid ex-addicts and healthy volunteers will be enrolled. Via the comprehensive assessments including clinical interview, neurocognitive examinations, electrocardiogram-based sleep breathing detector and pharmacogenomical evaluation, we will not only have the opportunities to have more insights on the impacts of opioid medications on sleep and neurocognitive performances, but also develop more adequate strategies to improve motivation and outcome in treating the opioid addicts.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Miaoli County, Taiwan, 35053
- National Health Research Institute
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ChangHua
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Lukang, ChangHua, Taiwan, 50550
- Changhua Christian Hospital
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New Taipei
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Banqiao, New Taipei, Taiwan, 22060
- Far Eastern Memorial Hospital
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Sanxia, New Taipei, Taiwan, 23702
- En-Chu-Gong Hospital
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New Taipei City
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Banqiao, New Taipei City, Taiwan, 22060
- Far Eastern Memorial Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Normal control group:
Healthy adults will be recruited from community.
- Methadone Maintenance treatment group Study subjects will be enrolled only in the methadone clinic.
- Buprenorphine/Naloxone treatment group Subjects will be enrolled only in the clinic.
- Drug-free ex-addict group Subjects will be recruited from the therapeutic communities and halfway house of Operation Dawn.
Description
Normal control group (NC):
Inclusion criteria:
- Chinese ethnicity
- Men or women above age of 20
- Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)
- Individuals who have completed a written consent form
Exclusion criteria:
Patients with comorbid severe mental disorders including:
- Organic mental disorders, or
- Schizophrenia
- Past diagnosis of Heroin dependence by DSM-IV definition
- Severe cognitive impairment
- Being pregnant
Methadone maintenance treatment group (MMT)
Inclusion criteria:
- Chinese ethnicity
- Men or women above age of 20, below age of 65
- Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)
- Diagnosis of Heroin dependence by DSM-IV definition
- Enter methadone maintenance therapy for at least 3 months
- No change of methadone dosage for the last week
- Regularly took methadone for the last week
- Individuals who have completed a written consent form
Exclusion criteria:
Patients with comorbid severe mental disorders including:
- Organic mental disorders, or
- Schizophrenia
- Severe cognitive impairment
- Being pregnant
Buprenorphine/Naloxone treatment group (BNT)
Inclusion criteria:
- Chinese ethnicity
- Men or women above age of 20, below age of 65
- Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)
- Diagnosis of Heroin dependence by DSM-IV definition
- Enter buprenorphine maintenance therapy for at least 3 months
- No change of buprenorphine dosage for the last week
- Regularly took buprenorphine for the last week
- Individuals who have completed a written consent form
Exclusion criteria:
Patients with comorbid severe mental disorders including:
- Organic mental disorders, or
- Schizophrenia
- Severe cognitive impairment
- Being pregnant
- Medication-free ex-addict group (MF)
Inclusion criteria:
- Chinese ethnicity
- Men or women above age of 20
- Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)
- Diagnosis of Heroin dependence by DSM-IV definition
- Individuals who have completed a written consent form
Exclusion criteria:
Patients with comorbid severe mental disorders including:
- Organic mental disorders, or
- Schizophrenia
- Severe cognitive impairment
- Being pregnant
- Exposure of methadone, buprenorphine and other opioid treatment in the previous 3 months
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Methadone maintenance treatment (MMT)
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Buprenorphine-Naloxone treatment (BNT)
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Medication-free ex-addicts(MF)
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Normal control (NC)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Group differences in demopraphics
Time Frame: one year
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support system, vital sign, substance use history
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one year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Gruop differences in neuro-cognitive functions
Time Frame: one year
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attention, executive function, decision making
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one year
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Collaborators and Investigators
Investigators
- Principal Investigator: Sheng-Chang Wang, M.D., M.Sc., National Health Research Institutes, Taiwan
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MD098SCW01
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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