Heart patients get new hope: varenicline vs. nicotine patch in quitting smoking
NCT ID NCT00959972
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tested whether varenicline (Chantix) helps smokers with coronary heart disease quit better than the standard nicotine patch. Fifty motivated smokers who had a heart-related event were randomly assigned to one of the two treatments for 12 weeks. The main goal was to see who stayed smoke-free, confirmed by breath tests, during the final weeks of treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Varenicline (Chantix) and transdermal nicotine patch
- What this could lead to
- If varenicline works better than the patch, it could give heart patients a more effective way to quit smoking and reduce their risk of future heart problems.
- What could go wrong
- This is a small pilot study with only 50 participants, so results may not apply to everyone. The trial is already completed, and the findings may not lead to a change in standard care without larger studies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
50 people
The number who actually took part.
- Start date
-
Apr 2009
- Finished
-
Nov 2010
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * smoking at least 10 cigarettes/day in the month prior to admission * patient has been diagnosed with acute coronary syndrome (includes patients admitted for unstable angina or acute myocardial infarction), elective percutaneous coronary intervention, or coronary artery bypass surgery at any point in time * motivated to stop smoking * geographically available for follow-up visits (i.e., live within 1 hour of the study centre) Exclusion Criteria: * have been using NRT, Zyban (or Wellbutrin), and/or Champix for more than 72 hours * have serious cardiac arrhythmias (e.g., tachycardia), vasospastic disease (e.g., Buerger's disease, Prinzmetal's variant angina) * have severe renal impairment or are on dialysis * unable to read and understand English * patient is pregnant or breastfeeding or planning on becoming pregnant during the study period
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Ottawa Heart Institute
Ottawa, Ontario, K1Y 4W7, Canada
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