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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00061087
Other study ID # NIDA-011444-1,#4184R
Secondary ID R01DA0114444184R
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date February 1998
Est. completion date October 2004

Study information

Verified date April 2019
Source New York State Psychiatric Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to treat Adult Attention Deficit Hyperactivity Disorder (ADHD) in methadone patients.


Description:

This project is a three armed double-blind, placebo-controlled, randomized trial comparing the efficacy of MPH and BPR, relative to each other and to placebo, for treating persistent ADHD in methadone-maintained patients. One hundred and twenty subjects, will be randomized to receive either MPH, BPR, or placebo with equal probability. Randomization will be stratified by site, and whether or not cocaine is also being used. Efficacy will be measured by treatment retention, reduction in illicit drug use and drug craving, improvement of ADHD symptoms and overall functional status.


Recruitment information / eligibility

Status Completed
Enrollment 115
Est. completion date October 2004
Est. primary completion date October 2004
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Individuals who meet DSM-IV criteria for opiate dependence and are currently maintained on methadone

- Patients must meet DSM-IV criteria for persistent adult ADHD

- Must be on stable methadone dose for at least 3 weeks

- Individuals positive for HIV will not be excluded.

Exclusion Criteria:

- Patients meeting DSM-IV criteria for current psychiatric disorders (other than ADHD or substance abuse) which requires psychiatric intervention

- Patients who are physiologically dependent on either sedatives or alcohol such that they experience symptoms requiring medical attention during periods of abstinence or significant reduction in amount of use

- Individuals diagnosed with other forms of adult ADHD other than persistent, particularly substance-induced ADHD

- Those who have an unstable medical condition which might make participation hazardous, including but not restricted to: uncontrolled hypertension, (SBP >160, DBP>100, PULSE >110), uncontrolled liver disease, uncontrolled diabetes, acute hepatitis, uncontrolled heart disease as indicated by history or abnormal ECG, glaucoma, or history of urinary retention or seizures, or advanced AIDS will not be included

- Patients who are taking prescription psychotropic medications other than methadone

- Patients who have exhibited suicidal or homicidal behavior within the past two years

- Patients with known sensitivity to MPH or BPR

- Patients with cognitive impairment or who cannot read or understand the self-report assessment forms unaided or are so severely disabled they cannot comply with the requirements of the study.

- Patients unable to give full and informed consent

- Patients with a history of an eating disorder

- Patients recently convicted of a violent crime. (last two years)

- Nursing mothers and pregnant women

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Methylphenidate
Methylphenidate 80mg/day
Bupropion
Bupropion 400mg/day
Other:
Placebo
Placebo

Locations

Country Name City State
United States Research Foundation for Mental Hygiene, Inc. New York New York

Sponsors (2)

Lead Sponsor Collaborator
New York State Psychiatric Institute National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

References & Publications (2)

Brooks DJ, Vosburg SK, Evans SM, Levin FR. Assessment of cognitive functioning of methadone-maintenance patients: impact of adult ADHD and current cocaine dependence. J Addict Dis. 2006;25(4):15-25. — View Citation

Levin FR, Evans SM, Brooks DJ, Kalbag AS, Garawi F, Nunes EV. Treatment of methadone-maintained patients with adult ADHD: double-blind comparison of methylphenidate, bupropion and placebo. Drug Alcohol Depend. 2006 Feb 1;81(2):137-48. Epub 2005 Aug 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Cocaine use based on urine toxicology collected 3 times per week for 12 weeks of the trial or length of study participation
Primary ADHD symptom severity based on the ADHD Rating scale score measured once per week for 12 weeks or length of study participation
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