Full Text View
Tabular View
No Study Results Posted
Related Studies
Safety of Combining Modafinil and Nicotine Replacement Therapy in Treating Nicotine Dependent Adolescents
This study is currently recruiting participants.
Study NCT00258479   Information provided by National Institute on Drug Abuse (NIDA)
First Received: November 22, 2005   Last Updated: September 29, 2008   History of Changes

November 22, 2005
September 29, 2008
June 2003
March 2009   (final data collection date for primary outcome measure)
Safety of combination drug treatment and physiological response; measured after treatment with each dose combination [ Time Frame: laboratory session ] [ Designated as safety issue: Yes ]
Safety of combination drug treatment and physiological response; measured after each dose combination
Complete list of historical versions of study NCT00258479 on ClinicalTrials.gov Archive Site
 
 
 
Safety of Combining Modafinil and Nicotine Replacement Therapy in Treating Nicotine Dependent Adolescents
Modafinil and Nicotine in Adolescents: Phase I Trial

Nicotine is one of the most widely abused substances in the United States. Nicotine replacement therapy (NRT) is currently an effective treatment for nicotine dependence; however, even with NRT most people fail at quitting smoking after their first attempt. Modafinil is a promising drug that may be useful in treating nicotine dependent individuals. The purpose of this study is to evaluate the safety of the combination of modafinil and NRT in treating nicotine dependent adolescent smokers.

NRT is a critical part of treating nicotine withdrawal symptoms, such as cravings, sleeplessness, poor concentration, and anxiety. The addition of modafinil, a promising pharmacologic agent, may enhance the effectiveness of NRT by further reducing inattention and depressed mood. The purpose of this study is to examine the safety of using both modafinil and NRT in treating nicotine dependent adolescents. In addition, this study will examine the effects of modafinil and NRT, alone and in combination, on alleviating symptoms of inattention and depressed mood.

Participants in this 12-day dose escalation study will be tested under eight different dose conditions. Modafinil and NRT will first be tested alone; participants will be exposed to low doses prior to higher doses of medication. Various modafinil-NRT dose combinations will then be tested. Modafinil will be administered at 5 p.m. each day, and NRT will be self-administered at the start of each day in which a participant must complete lab tests. The following measures will be obtained at study visits occurring before and after the various modafinil-NRT dose combinations: nicotine withdrawal symptoms, medication side effects, activity level, cardiovascular response, and profile of mood states (POMS).

Phase I
Interventional
Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Single Group Assignment, Safety Study
Tobacco Use Disorder
  • Drug: Modafinil
  • Drug: Nicotine Replacement Therapy
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
100
March 2009
March 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Smokes 10 or more cigarettes per day

Exclusion Criteria:

  • Current use of any medication for a psychiatric disorder
  • Positive drug screen test
  • Uses smokeless tobacco
Both
16 Years to 40 Years
Yes
Contact: Catherine A. Martin, MD 859-257-9341 cmartin@uky.edu
United States
 
NCT00258479
Catherine A. Martin, University of Kentucky
NIDA-15413, R03DA15413, DPMC
National Institute on Drug Abuse (NIDA)
 
Study Chair: Catherine Martin, PhD University of Kentucky
National Institute on Drug Abuse (NIDA)
September 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP