A Study To Evaluate The Efficacy And Safety Of Varenicline Compared To Placebo For Smoking Cessation Through Reduction
- Registration Number
- NCT01370356
- Lead Sponsor
- Pfizer
- Brief Summary
This study will determine whether varenicline is safe and helps people to quit smoking through reduction when they are not willing/able to make an abrupt quit attempt.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 1510
- Male and female cigarette smokers over the age of 18 years who are not willing/able to quit smoking within the next month but who are willing to attempt to reduce their smoking to work toward a quit attempt within the next 3 months.
- Subjects must have smoked an average of at least 10 cigarettes per day during the past year and during the month prior to the screening visit, with no continuous period of abstinence greater than 3 months in the past year and who have an exhaled carbon monoxide (CO) >10 ppm at screening.
- Subjects with mild to moderate depression or anxiety may be included if their condition is stable.
- Subjects with a history of a suicide attempt or any suicidal behavior in the past two years.
- Subjects with severe depression or anxiety.
- Subjects with psychosis, panic disorder, bipolar disorder, post traumatic stress disorder (PTSD), or schizophrenia.
- Subjects with alcohol or substance abuse or dependence (except nicotine) unless in full remission for at least 12 months.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Varenicline Tartrate Varenicline Tartrate - Placebo Placebo -
- Primary Outcome Measures
Name Time Method Percentage of Participants With Carbon Monoxide (CO) Confirmed 10-Week Continuous Abstinence (CA) From Smoking Week 15 - 24 Percentage of participants who remained abstinent from Week 15 to Week 24, inclusive, reporting no smoking and no use of nicotine-containing products since the last study visit or contact on the Nicotine Use Inventory (NUI) and confirmed by expired CO \< 10 ppm at any time point (CO measurements conducted at the clinic visits) during Weeks 15 through 24, inclusive. Missing CO was imputed as negative (CO ≤ 10 ppm).
- Secondary Outcome Measures
Name Time Method Percentage of Participants With CO Confirmed 4-Week CA From Smoking Week 21 - 24 Percentage of participants who remained abstinent from Week 21 to Week 24, inclusive, reporting no smoking and no use of nicotine-containing products since the last study visit or contact on the NUI and confirmed by expired CO \< 10 ppm at any time point (CO measurements conducted at the clinic visits) during Weeks 21 through 24, inclusive. Missing CO was imputed as negative (CO ≤ 10 ppm).
Percentage of Participants With CO Confirmed Long Term CA From Smoking Weeks 21 - 52 Percentage of participants who remained abstinent from Week 21 to Week 52, inclusive, reporting no smoking and no use of nicotine-containing products since the last study visit or contact on the NUI and confirmed by expired CO \< 10 ppm at any time point (CO measurements conducted at the clinic visits) during Weeks 21 through 52, inclusive. Missing CO was imputed as negative (CO ≤ 10 ppm).
Percentage of Participants With 7-Day Point Prevalence of Smoking Cessation Week 12, 24, and 52 The 7-day point prevalence of abstinence was defined as being abstinent from smoking and using tobacco products during the last 7 days at Week 12, 24, and 52. The participant's smoking status and other nicotine use was evaluated based on the "last 7 days" questions on the NUI and confirmed by CO expiration. Responders were defined as those, who answered "no" to both questions ("Has the subject smoked any cigarettes (even a puff) in the last 7 days?"; and "Has the subject used any nicotine products and/or other tobacco.... in the last 7 days?") and whose expired CO \< 10 ppm. Missing CO was imputed as negative (CO ≤ 10 ppm).
Percentage of Participants With 4-Week Point Prevalence of Smoking Cessation Week 52 The 4-week point prevalence of abstinence was defined as being abstinent from smoking and using tobacco products during the last 4 weeks of the study. The participant's smoking status and other nicotine use was evaluated based on the "last 4 weeks" questions on the NUI and confirmed by CO expiration. Responders were defined as those, who answered "no" to both questions ("Has the subject smoked any cigarettes (even a puff) in the last 4 weeks?"; and "Has the subject used any nicotine products and/or other tobacco.... in the last 4 weeks?") and whose expired CO \< 10 ppm. Missing CO was imputed as negative (CO ≤ 10 ppm).
Trial Locations
- Locations (63)
Royal Brisbane and Women's Hospital
🇦🇺Herston, Queensland, Australia
Office of Dr. Ronald Collette
🇨🇦Burnaby, British Columbia, Canada
The Alverton Practice
🇬🇧Penzance, Cornwall, United Kingdom
Knowle House Surgery
🇬🇧Plymouth, Devon, United Kingdom
Vseobecna fakultni nemocnice v Praze
🇨🇿Praha 2, Czech Republic
National Cheng Kung University Hospital
🇨🇳Tainan, Taiwan
Castlemilk Health Centre
🇬🇧Castlemilk, Glasgow, United Kingdom
Taipei Veterans General Hospital
🇨🇳Taipei, Taiwan
Clinica de Enfermedades Cronicas y de Procedimientos Especiales S.C.
🇲🇽Morelia, Michoacan, Mexico
Healthfirst Medical Group
🇺🇸Fort Worth, Texas, United States
Canadian Phase Onward Inc.
🇨🇦Toronto, Ontario, Canada
Mestska nemocnice Ostrava, Plicni oddeleni
🇨🇿Ostrava 1, Czech Republic
Ain Shams University Hospital
🇪🇬Cairo, Egypt
Ustredni vojenska nemocnice Praha
🇨🇿Praha 6, Czech Republic
Pharmacology Research Institute
🇺🇸Newport Beach, California, United States
Manna Research
🇨🇦Toronto, Ontario, Canada
Fakultni nemocnice u sv. Anny v Brne
🇨🇿Brno, Czech Republic
Krajska nemocnice Liberec a.s., Plicni oddeleni
🇨🇿Liberec 1, Czech Republic
Arke Estudios Clinicos S.A.
🇲🇽Mexico, D.f., Mexico
Centro de Estudios Clinicos y Especialidades Medicas SC
🇲🇽Monterrey, Nuevo Leon, Mexico
El Fayoum university hospital
🇪🇬El Fayoum, Egypt
Clinique des Maladies Lipidiques de Quebec (CMLQ)
🇨🇦Quebec, Canada
Klinische Forschung Berlin-Buch GmbH
🇩🇪Berlin, Germany
National Taiwan University Hospital, Department of Family Medicine
🇨🇳Taipei, Taiwan
SurGal Clinic s.r.o.
🇨🇿Brno, Czech Republic
Australian Clinical Research Network
🇦🇺Maroubra, New South Wales, Australia
Brisbane South Clinical Research Centre
🇦🇺Carina Heights, Queensland, Australia
James K. Lai, MD., Inc.
🇨🇦Vancouver, British Columbia, Canada
White Hills Medical Clinic
🇨🇦St. John's, Newfoundland and Labrador, Canada
Klinische Forschung Hamburg GmbH
🇩🇪Hamburg, Germany
Tajima Clinic
🇯🇵Edogawa-ku, Tokyo, Japan
Nagatsuta family clinic
🇯🇵Yokohama, Kanagawa, Japan
Enchord Limited
🇬🇧Fowey, Cornwall, United Kingdom
Sakakibara Clinic, Wakaumekai Medical Corporation
🇯🇵Yokohama, Kanagawa, Japan
Medamed- Studienambulanz
🇩🇪Leipzig, Germany
FOCUS Clinical Drug Development GmbH
🇩🇪Neuss, Germany
Clinical Neuroscience Solutions, Inc.
🇺🇸Orlando, Florida, United States
Central Kentucky Research Associates, Inc.
🇺🇸Lexington, Kentucky, United States
The Center for Pharmaceutical Research, P.C.
🇺🇸Kansas City, Missouri, United States
FutureSearch Clinical Trials, L.P.
🇺🇸Austin, Texas, United States
Central New York Clinical Research
🇺🇸Manlius, New York, United States
Vseobecna fakultni nemocnice v Praze, III. interni klinika
🇨🇿Praha 2, Czech Republic
Emeritus Research
🇦🇺Malvern, Victoria, Australia
Alexandria University
🇪🇬Alexandria, Egypt
Klinische Forschung Berlin
🇩🇪Berlin, Germany
Universitaetsklinikum Goettingen Zentrum Innere Medizin Abteilung Kardiologie und Pneumologie
🇩🇪Goettingen, Germany
Universitaetsklinikum Goettingen, Zentrum Innere Medizin, Abteilung Kardiologie und Pneumologie
🇩🇪Goettingen, Germany
Saino Clinic
🇯🇵Tokorozawa, Saitama, Japan
Hachiouji Junkanki clinic
🇯🇵Hachiouji, Tokyo, Japan
Kubo Clinic
🇯🇵Yokohama, Kanagawa, Japan
Chang Gung Medical Foundation-Linkou Branch
🇨🇳Kweishan Town, Taoyuan County, Taiwan
China Medical University Hospital
🇨🇳Taichung, Taiwan
Centro Respiratorio de Mexico S.C.
🇲🇽Mexico, D.f., Mexico
Kaohsiung Veterans General Hosptial
🇨🇳Kaohsiung, Taiwan
Taichung Veterans General Hospital
🇨🇳Taichung, Taiwan
Prince Philip Hospital
🇬🇧Dafen, Llanelli, United Kingdom
Hathaway Medical Centre
🇬🇧Chippenham, Wilts, United Kingdom
The Jenner Practice
🇬🇧London, United Kingdom
University of Nebraska Medical Center
🇺🇸Omaha, Nebraska, United States
CRI Worldwide, LLC
🇺🇸Marlton, New Jersey, United States
Clinical Research Integrity(CRI) Worldwide, LLC
🇺🇸Willingboro, New Jersey, United States
Mayo Clinic
🇺🇸Rochester, Minnesota, United States
Benchmark Research
🇺🇸Fort Worth, Texas, United States