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Treatment of Adult Attention Deficit Hyperactivity Disorder (ADHD) in Methadone Patients - 1

Treatment of Adult ADHD in Methadone Patients

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00061087
Enrollment
115
Registered
2003-05-22
Start date
1998-02-28
Completion date
2004-10-31
Last updated
2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ADHD, Cocaine Dependence, Opioid-Related Disorders

Keywords

ADHD, Cocaine, Treatment, Methadone

Brief summary

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

Detailed 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.

Interventions

DRUGMethylphenidate

Methylphenidate 80mg/day

DRUGBupropion

Bupropion 400mg/day

OTHERPlacebo

Placebo

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
New York State Psychiatric Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Cocaine use based on urine toxicologycollected 3 times per week for 12 weeks of the trial or length of study participation
ADHD symptom severity based on the ADHD Rating scale scoremeasured once per week for 12 weeks or length of study participation

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026