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PHARMACOTHERAPIES: EFFICACY, MECHANISMS, AND ALGORITHMS - 1 - Article


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Nicotine Skin Patches

Habitrol; NicoDerm; Nicotine transdermal system; Nicotrol; ProStep 




Clinical Trial: PHARMACOTHERAPIES: EFFICACY, MECHANISMS, AND ALGORITHMS - 1

This study is not yet open for patient recruitment.

Sponsored by: National Institute on Drug Abuse (NIDA)
Information provided by: National Institute on Drug Abuse (NIDA)

Purpose

. The proposed work will advance the understanding and effectiveness of tobacco dependence treatment and result in more smokers quitting successfully.

Condition Treatment or Intervention Phase
nicotine
 Drug: nicotine
Phase I

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Treatment, Placebo Control

Official Title: PHARMACOTHERAPIES: EFFICACY, MECHANISMS, AND ALGORITHMS

Further Study Details: 

Study start: September 2004;  Expected completion: February 2010

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Smoke at least 10 cigarettes per day for the previous 6 months
  • Expired CO > 9 ppm
  • Motivated to quit smoking
  • Able to read and write English
  • Willing to complete required study assessments

Exclusion Criteria:

  • Uncontrolled hypertension (systolic >180mm Hg or diastolic >110mm Hg)
  • History of bipolar disorder or psychosis
  • Myocardial infarction or other serious cardiac problem in the previous 4 weeks
  • History of diagnosed anorexia and/or bulimia
  • Diagnosis of Alcohol Dependence in the previous 6 months by participant self-report or drinking 6 or more drinks on six or more days a week
  • History of seizure and/or serious head injury involving loss of consciousness
  • Use of contraindicated medications (MAO inhibitors, bupropion, lithium, anticonvulsants, antipsychotics)
  • Currently pregnant or breast-feeding
  • Unwilling to use effective contraception during the treatment phase
  • More than one participant from the same household
  • Allergic reactions to 3 or more classes of drugs

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00109447

David Fraser, M.S.      (608)265-4561    dlf@ctri.medicine.wisc.edu

Wisconsin
      UW-CTRI Madison Research site, Madison,  Wisconsin,  53711 2027,  United States
Daniel Lawrence, Ph.D.  608-262-8568    dll@ctri.medicine.wisc.edu 

      UW-CTRI Milwaukee Research site, Milwaukee,  Wisconsin,  53233,  United States
Patricia Weston, M.S.W  414-219-6535    pw3@ctri.medicine.wisc.edu 

Study chairs or principal investigators

Timothy Baker, Ph.D.,  Principal Investigator,  University of Wisconsin-Madison   

More Information

Study ID Numbers:  NIDA-19706-1; P50-19706-1
Record last reviewed:  April 2005
Last Updated:  April 27, 2005
Record first received:  April 27, 2005
ClinicalTrials.gov Identifier:  NCT00109447
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-05-03


Source: ClinicalTrials.gov
Cache Date: May 4, 2005

Resources



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December 5, 2009



Page Updated: June 1, 2005
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