NCT Number: NCT00067158
Smoking Cessation Treatment With Transdermal Nicotine Replacement Therapy - 1
The purpose of this study is to look at how feasible it is to incorporate a state-of-the-art smoking cessation treatment program into community substance abuse treatment programs and its impact on substance abuse and cigarette smoking.
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Notify MeKey information
Conditions
Age range
18 year–99 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Matrix Institute on Addictions, Los Angeles, California, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patient is alcohol or drug dependent, in Outpatient Drug-Free or Opiate Substitute program and is interested in quitting smoking
Exclusion criteria
- Patient is psychotic
- Use of smokeless tobacco
- Use of other smoking cessasation product
- Pregnancy
- Patient has hyper-tension, heart problems, or skin condition
Treatment and study plan
Primary outcomes
-
Drug use
-
Smoking Cessation
Sponsors and collaborators
Lead sponsor
New York University
Other
Registry information
Official study title
Smoking Cessation Treatment With Transdermal Nicotine Replacement Therapy
Important dates
- Study start
- 2003
- Primary completion
- 2004
- Study completion
- 2004
- First posted
- Aug 13, 2003
- Registry last updated
- Jan 12, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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