Atomoxetine for Treating Cocaine Abuse in Adults With Attention Deficit Hyperactivity Disorder (ADHD)

Phase 2

Completed

Conditions: Attention Deficit Disorder With Hyperactivity
Cocaine-Related Disorders

Interventions: Drug: Atomoxetine

Registration Number: NCT00218543

Lead Sponsor: New York State Psychiatric Institute

Brief Summary: Studies have shown that individuals with attention deficit hyperactivity disorder (ADHD) are at greater risk for having a substance use disorder compared to people who do not have ADHD. Rates of cocaine abuse in adults with ADHD are significantly higher than they are in adults who do not have ADHD. Some clinicians suggest that adults with ADHD may abuse cocaine in order to self-medicate their ADHD symptoms. Atomoxetine is a drug that has been effective in treating ADHD. This study will evaluate the effectiveness of atomoxetine in reducing cocaine use in people with ADHD who abuse cocaine.

Detailed Description: ADHD is a neurologic disorder that is thought to be caused by chemical imbalances of certain neurotransmitters in the brain. The disorder can cause inattention, hyperactivity, and impulsivity. Cocaine abuse rates in adults with ADHD are significantly higher than they are in adults who do not have the disorder. This may be reflective of an attempt by individuals with ADHD to self-treat symptoms. Atomoxetine is an FDA-approved drug that is used to increase the ability to pay attention and decrease impulsiveness and hyperactivity in children and adults with ADHD. The drug is in a class of medications called selective norepinephrine reuptake inhibitors and works by increasing the levels of norepinephrine, a natural substance in the brain that affects a person's attention and impulsivity. It is possible that reducing ADHD symptoms in cocaine abusers with ADHD will help decrease their need for cocaine. This study will evaluate the effectiveness of atomoxetine in reducing cocaine use in people with ADHD who abuse cocaine.

Participants in this open label study will receive atomoxetine for 12 weeks, and will take one dose each morning for the duration of the study. Doses will be increased gradually to minimize side effects and enhance treatment compliance. In addition, all participants will receive individualized relapse prevention therapy once weekly. Participants will be required to report to the study site three times a week to receive medication, complete questionnaires regarding ADHD symptoms and substance use behavior, and provide a urine sample while being supervised by study staff. Also, vital signs will be monitored and medication side effects will be assessed at each visit. Participants will report to the study site 6 months after starting in the study for a follow-up visit, at which time ADHD symptoms, substance use behavior, and social functioning will be assessed.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 20

Inclusion Criteria

Meets DSM-IV criteria for cocaine dependence and adult ADHD
Describes cocaine as the primary drug of abuse
Meets DSM-IV criteria for cocaine dependence

Exclusion Criteria

Meets DSM-IV criteria for current Axis I psychiatric disorders that require a psychiatric intervention (except ADHD or substance abuse)
Current major depression
Unstable physical disorders that might make participation unsafe (e.g., uncontrolled high blood pressure and tachycardia [systolic blood pressure greater than 150 mm Hg, diastolic blood pressure greater than 90 mm Hg, or a sitting heart rate greater than 100])
Acute hepatitis (individuals with chronic mildly elevated transaminase levels of less than 2 or 3 times the normal limit are not excluded)
Diabetes
Coronary vascular disease, as indicated by a history or suspected by an abnormal electrocardiogram
History of cardiac symptoms
History of seizures
Narrow angle glaucoma
Use of monoamine oxidase inhibitors (MAOIs) within 2 weeks of starting treatment with atomoxetine
Currently taking prescribed psychotropic medications
Currently taking medications for the treatment of ADHD
Known sensitivity to atomoxetine
Current suicidal ideation or history of suicidal or homicidal behavior within 2 years prior to study entry
Pregnant or breastfeeding
Physiologically dependent on any drugs other than nicotine or marijuana
History of schizophrenia, bipolar disorder, or other psychotic disorders
Currently taking cough medicine (e.g., dextromethorphan) and/or albuterol

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Atomoxetine	Atomoxetine	Atomoxetine

Primary Outcome Measures

Name	Time	Method
ADHD Symptoms Based on Adult ADHD Rating Scale Scale (AARS)	measured during 12 weeks or length of study participation	Weekly AARS scores (continuous, range 0-54) were examined with the baseline score compared to that at the last assessment obtained and change in these scores over time. The AARS looks at adult ADHD symptoms. A score of 0 represents no symptoms and 54 would be indicative of the most severe level of symptoms.
the Adult ADHD Rating Scale (AARS) (30% Reduction)	baseline compared to rating at week 12 or last rating during study participation	AARS is a self report that measures symptoms of adult ADHD. The primary outcome was the percentage of patients achieving a 30% reduction from baseline on the AARS scale. The AARS is scored on a continuous, range 0-54. 0 being no symptoms and 54 being indicative of the most severe level of symptoms.

Secondary Outcome Measures