An Alternative Dosing Schedule of Varenicline for Smoking Cessation
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT00835900 |
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Recruitment Status :
Completed
First Posted : February 4, 2009
Results First Posted : May 30, 2017
Last Update Posted : May 30, 2017
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Smoking Cessation | Drug: varenicline Drug: placebo | Phase 2 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 60 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Triple (Participant, Investigator, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Extended Varenicline for Smoking Cessation: A Pilot Study |
| Study Start Date : | March 2009 |
| Actual Primary Completion Date : | July 2010 |
| Actual Study Completion Date : | July 2015 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: varenicline
drug plus counseling.
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Drug: varenicline
variable dosing schedule
Other Name: Chantix |
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Active Comparator: placebo
placebo plus counseling
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Drug: placebo
placebo |
- Change in Smoking Behavior [ Time Frame: Change in cigarettes per day from Week 2 to Week 5 ]Change in cigarettes per day from Week 2 to Week 5
- Rates of Smoking Cessation. [ Time Frame: 12 weeks after quit date. ]To parallel most clinical trials of varenicline, we focused on CO-verified (<11 parts per million) continuous abstinence (not even one puff) during the final 4 weeks of treatment (i.e., post-quit weeks 8 through 11). Participants lost to follow-up were coded as smokers.
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| Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- currently smoking at least 15 cigarettes daily
- in good health
- able to read and speak English fluently
- have a home telephone and plan to reside in Western New York for 6 months
- willing to make quit attempt
- signed informed consent
- who planned quit attempt.
Exclusion Criteria:
- serious medical condition
- depression or mental health condition requiring treatment in the past year
- history of panic disorder, psychosis, bipolar disorder
- alcohol or drug abuse in the past year
- use of tobacco products other than cigarettes
- current use of other cessation pharmacotherapies
- pregnancy/planned pregnancy.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00835900
| United States, New York | |
| Roswell Park Cancer Institute | |
| Buffalo, New York, United States, 14263 | |
| Principal Investigator: | Martin C Mahoney, MD, PhD | Roswell Park Cancer Institute |
| Responsible Party: | Roswell Park Cancer Institute |
| ClinicalTrials.gov Identifier: | NCT00835900 |
| Obsolete Identifiers: | NCT00957515 |
| Other Study ID Numbers: |
I 136208 Pfizer IIR-GA30523 |
| First Posted: | February 4, 2009 Key Record Dates |
| Results First Posted: | May 30, 2017 |
| Last Update Posted: | May 30, 2017 |
| Last Verified: | April 2017 |
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smoking cessation varenicline smoking cessation treatment |
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Varenicline Nicotinic Agonists Cholinergic Agonists Cholinergic Agents |
Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs |

