Pharmacogenomics Study of Sleep Disturbance and Neurocognitive Impairments in the Opioid Addicts

Heroin Dependence Clinical Trial

Official title:

Pharmacogenomics Study of Sleep Disturbance and Neurocognitive Impairments in the Opioid Addicts

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01668706
• Other study ID #: MD098SCW01
• Status: Completed
• Phase: N/A
• First received: August 16, 2012
• Last updated: November 8, 2016
• Start date: March 2009
• Est. completion date: December 2013

Study information

• Verified date: August 2012
• Source: National Health Research Institutes, Taiwan
• Contact: n/a
• Is FDA regulated: No
• Health authority: Taiwan: National Health Research Institutes
• Study type: Observational

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 340
• Est. completion date: December 2013
• Est. primary completion date: December 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 20 Years to 65 Years

Eligibility

1. Normal control group (NC):

Inclusion criteria:

1. Chinese ethnicity

2. Men or women above age of 20

3. Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)

4. Individuals who have completed a written consent form

Exclusion criteria:

1. Patients with comorbid severe mental disorders including:

1. Organic mental disorders, or

2. Schizophrenia

2. Past diagnosis of Heroin dependence by DSM-IV definition

3. Severe cognitive impairment

4. Being pregnant

2. Methadone maintenance treatment group (MMT)

Inclusion criteria:

1. Chinese ethnicity

2. Men or women above age of 20, below age of 65

3. Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)

4. Diagnosis of Heroin dependence by DSM-IV definition

5. Enter methadone maintenance therapy for at least 3 months

6. No change of methadone dosage for the last week

7. Regularly took methadone for the last week

8. Individuals who have completed a written consent form

Exclusion criteria:

1. Patients with comorbid severe mental disorders including:

1. Organic mental disorders, or

2. Schizophrenia

2. Severe cognitive impairment

3. Being pregnant

3. Buprenorphine/Naloxone treatment group (BNT)

Inclusion criteria:

1. Chinese ethnicity

2. Men or women above age of 20, below age of 65

3. Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)

4. Diagnosis of Heroin dependence by DSM-IV definition

5. Enter buprenorphine maintenance therapy for at least 3 months

6. No change of buprenorphine dosage for the last week

7. Regularly took buprenorphine for the last week

8. Individuals who have completed a written consent form

Exclusion criteria:

1. Patients with comorbid severe mental disorders including:

1. Organic mental disorders, or

2. Schizophrenia

2. Severe cognitive impairment

3. Being pregnant

4. Medication-free ex-addict group (MF)

Inclusion criteria:

1. Chinese ethnicity

2. Men or women above age of 20

3. Able to participate in a clinical assessment in Chinese (including Mandarin and Taiwanese dialects)

4. Diagnosis of Heroin dependence by DSM-IV definition

5. Individuals who have completed a written consent form

Exclusion criteria:

1. Patients with comorbid severe mental disorders including:

1. Organic mental disorders, or

2. Schizophrenia

2. Severe cognitive impairment

3. Being pregnant

4. Exposure of methadone, buprenorphine and other opioid treatment in the previous 3 months

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Dyssomnias
• Heroin Dependence
• Parasomnias
• Sleep Wake Disorders

Locations

Country	Name	City	State
Taiwan	Far Eastern Memorial Hospital	Banqiao	New Taipei City
Taiwan	Far Eastern Memorial Hospital	Banqiao	New Taipei
Taiwan	ChangHua Christian Hospital	Lukang	ChangHua
Taiwan	National Health Research Institute	Miaoli County
Taiwan	En-Chu-Gong Hospital	Sanxia	New Taipei

Sponsors (1)

Lead Sponsor	Collaborator
National Health Research Institutes, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Group differences in demopraphics	support system, vital sign, substance use history	one year	No
Secondary	Gruop differences in neuro-cognitive functions	attention, executive function, decision making	one year	No