Expired Study
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Cincinnati, Ohio 45220


Purpose:

The purpose of this study is to demonstrate the feasibility of methylphenidate (MPD) as effective and safe in the outpatient treatment of cocaine-dependent patients with a comorbid DSM-IV diagnosis of Attention Deficit Hyperactivity Disorder (ADHD), to demonstrate the ability of each site to participate in a subsequent anticipated controlled trial of MPD (recruitment and execution), and to gather preliminary data on the ability of sweat patches to detect episodes of cocaine use.


Study summary:

Forty-one participants were enrolled into this multi-site, outpatient, open-label, ten-week trial. Participants were scheduled to attend three visits per week to allow safety and efficacy measures to be taken. In addition, participants were given two hours of individual substance abuse therapy during the first four weeks, and one hour per week during the last six weeks, of the trial. All participants were started on a total daily dose of 20 mg MPD. The total daily dose was then increased to a maximum daily dose of 60 mg (20 mg TID) or to the maximum dose tolerated by the participant.


Criteria:

Inclusion Criteria: 1. Subject must be between 21 and 50 years of age, male or female, of any race. 2. If female, subject cannot be pregnant or lactating. 3. Subject must be cocaine-dependent (as determined by the SCID and a clinical interview by a psychiatrist). 4. Subject must meet DSM-IV diagnostic criteria for ADHD: 5. Subject must have been actively using cocaine, (BE>300 ng/ml) within 30 days of the screening examination. 6. Subject must be negative for cocaine metabolites immediately prior to receiving a study treatment number and initial dose of MPD, as determined first by urine testing kit with result later confirmed by laboratory urine toxicology (BE < 300 ng/ml). 7. Subject must be willing and able to give informed consent. Exclusion Criteria: 1. Subject has symptoms of AIDS. 2. Subject has a chronic medical disorder requiring medication. 3. Subject has a SCID Axis-I psychiatric diagnosis requiring medication. 4. Subject meets DSM-IV criteria for dependence for any substance except cocaine, alcohol, nicotine, marijuana, caffeine, and has been actively using during the past two weeks. 5. Subject is in need of detoxification from alcohol or benzodiazepines 6. Subject is taking psychotropic medication (except chloral hydrate for insomnia). 7. Subject is female of childbearing age who is at risk for becoming pregnant and is not using adequate contraceptive techniques as determined by the evaluating physician or Principal Investigator. 8. Subject has ALT or AST levels above three times laboratory normal 9. Subject has renal function tests (creatinine and BUN) or electrolyte levels (K, Na, Cl, HCO3) that are not within normal limits at baseline. 10. Subject has an EKG indicating clinically significant arrhythmias or abnormal conduction 11. Subject has organic brain syndrome (OBS) as evidenced in the psychiatric evaluation. 12. Subject has an acute or chronic medical or psychiatric condition which in the judgment of the evaluating physician would make study participation difficult or unsafe. 13. Subject has been enrolled in another research protocol within the past 45 days. 14. Subject has narrow angle glaucoma, by history 15. Subject has a diagnosis or family history of Tourettes syndrome 16. Subject has a history of seizures or seizure disorder 17. Subject has had an adverse reaction to methylphenidate 18. Subject has abnormal thyroid function (as determined by an abnormal T4 level that is clinically significant) 19. Subject has been treated for ADHD with psychomotor stimulants within the past month. 20. Subject plans to receive psychosocial treatment external to that designated in the protocol during study participation.


NCT ID:

NCT00015054


Primary Contact:

Principal Investigator
Eugene Somoza, M.D., Ph.D.
Cincinnati MDRU


Backup Contact:

N/A


Location Contact:

Cincinnati, Ohio 45220
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 22, 2017

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