Methylphenidate Treatment for Cocaine Abuse and ADHD - 1
Information source: National Institute on Drug Abuse (NIDA)
Information obtained from ClinicalTrials.gov on December 31, 2007 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Attention Deficit Disorder With Hyperactivity; Cocaine-Related Disorders
Intervention: Methylphenidate (Drug)
Phase: Phase 1
Status: Active, not recruiting
Sponsored by: National Institute on Drug Abuse (NIDA) Official(s) and/or principal investigator(s): Frances R Levin, M.D., Principal Investigator, Affiliation: Research Foundation for Mental Hygiene, Inc.
Summary
Many cocaine dependent individuals are also diagnosed with Attention Deficit Hyperactivity
Disorder (ADHD). Methylphenidate (Ritalin) is currently approved to treat individuals
diagnosed with ADHD. The purpose of this study is to determine the effectiveness of
methylphenidate in treating ADHD symptoms in cocaine dependent individuals.
Clinical Details
Official title: Methylphenidate Treatment for Cocaine Abuse and ADHD
Study design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: ADHD symptom severity, Week 14
Detailed description:
Methylphenidate (MPH) is commonly used to treat individuals diagnosed with ADHD. The
purpose of this study is to determine the effectiveness of MPH in treating adult cocaine
dependent individuals who are also diagnosed with ADHD.
Participants in this 14-week, double-blind, placebo-controlled study will be randomly
assigned to receive either sustained-release MPH or placebo. All participants will receive
individual cognitive behavioral therapy. The trial will last 14 weeks. It will include a
1-week placebo lead-in phase and a 2-week dose titration phase, followed by 11 weeks on a
stable dose of MPH. During the titration phase, MPH will be given twice a day, starting at a
dose of 10 mg/day. The dose will increase by 10 mg each day, until a final stable dose of 40
mg/day is reached. At this time, sustained-release MPH will be given as two 20 mg doses (one
in the morning and one in the afternoon). Depending on a participant's tolerance of MPH, the
dose will be increased to a maximum of 60 mg/day (40 mg in the morning and 20 mg in the
afternoon). Participants who are unable to tolerate a dose of at least 40 mg/day of MPH will
be discontinued from the study. Assessments of ADHD symptoms will be completed at weekly
study visits. In addition, drug use assessments will also be completed and will include
self-reports and urine toxicology tests.
Eligibility
Minimum age: 18 Years.
Maximum age: 60 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
Meets DSM-IV criteria for cocaine dependence
Meets DSM-IV criteria for persistent adult Attention Deficit Hyperactive
Disorder
Exclusion Criteria:
Meets DSM-IV criteria for current psychiatric disorders (other than ADHD or substance
abuse) that requires a psychiatric intervention
Physiologically dependent on sedatives or alcohol, to the extent that medical attention is
required during periods of abstinence or significant reduction in the amount of
use
Exhibits suicidal or homicidal behavior within the two years prior to enrollment
Currently taking prescription psychotropic medication
Unstable medical condition (e. g., uncontrolled diabetes) that would make participation in
the study hazardous
Known sensitivity to methylphenidate
Pregnant or breastfeeding
Locations and Contacts
Research Foundation for Mental Hygiene, Inc., New York, New York 10032, United States
Additional Information
Starting date: April 1998
Ending date: March 2004
Last updated: April 11, 2007
|