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Updated May 2026 · ClinicalTrials.gov

RECRUITINGPhase 3INTERVENTIONAL

Aggressive Smoking Cessation Trial (ASAP)

Aggressive Smoking Cessation Therapy Among People at Elevated Cardiovascular Risk (ASAP) Trial

Aggressive Smoking Cessation Trial (ASAP) (NCT05257629) is a Phase 3 interventional studying Acute Coronary Syndrome and Cardiovascular Diseases, sponsored by Sir Mortimer B. Davis - Jewish General Hospital. RECRUITING as of the most recent ClinicalTrials.gov update. Talk to your doctor before contacting the trial site.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The ASAP Trial is a 5-year, multi-centre, randomized controlled trial that will assess the efficacy, safety, and tolerability of aggressive smoking cessation therapy among people at elevated cardiovascular risk. It will recruit 798 adult patients smoking on average at least 10 conventional (tobacco) cigarettes per day who are motivated to quit smoking and have either been diagnosed with ACS requiring hospitalization or are outpatients at elevated cardiovascular risk. Patients will be randomized (1:1) to one of two treatment arms: (1) combination therapy of varenicline and nicotine e-cigarettes plus counseling or (2) varenicline plus counseling for 12 weeks, with 52-week follow-up.

What Stage of Research Is This?

Phase 3 trials confirm efficacy and safety in large patient groups (often 300–3,000+) and form the evidence base for an FDA approval submission. For Acute Coronary Syndrome, Phase 3 studies typically randomize participants between the investigational treatment and either a placebo or current standard of care. A successful Phase 3 result is the threshold most treatments need to clear before regulatory approval.

This trial is currently recruiting participants. The sponsor has registered the study with ClinicalTrials.gov as actively enrolling, which means new applicants who meet the eligibility criteria can be considered for screening. Trial status can change between updates — confirm current recruiting status with the study contact before traveling for a screening visit.

A target enrollment of 798 participants makes this a sizable late-stage trial. Studies in this range typically have enough power to detect clinically meaningful differences from a comparator and to characterize less-common side effects.

Who May Be Eligible (Plain English)

Who May Qualify: 1. Patients currently hospitalized or being discharged from hospital who have suffered an ACS, defined as follows: i. MI, defined by positive troponin T, troponin I, or CK-MB levels (as defined by institution-specific cut-offs) and ≥ 1 of the following: 1. Ischemic symptoms for ≥ 20 min; 2. Electrocardiogram (ECG) changes indicative of ischemia (ST-segment elevation or depression); 3. Development of pathological Q waves on the ECG ii. Unstable angina with significant coronary artery disease, defined by all of the following: 1. Ischemic symptoms for ≥ 20 min; 2. ECG changes indicative of ischemia (ST-segment changes); 3. At least one lesion ≥ 50% on angiogram performed during the current hospitalization. \[Note: patients who undergo cardiac catheterization or percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG) surgery will be eligible provided they are able to start varenicline in-hospital and nicotine e-cigarette at discharge.\] OR Outpatients with the following diagnoses/conditions: i. Cardiovascular: 1. Coronary artery disease documented with angiography or coronary CT; 2. Previous ACS, MI, stable or UA; 3. Previous coronary revascularization (e.g. PCI or CABG). ii. Renovascular: a. Chronic kidney disease. iii. Cerebrovascular: a. Previous cerebral infarction or transient cerebral ischemic attack. iv. Peripheral vascular: 1. Abdominal aortic aneurysm \> 3.0 cm or previous aortic aneurysm surgery; 2. Ankle-brachial pressure index of \< 0.9 or intermittent claudication; 3. Documented carotid artery disease; 4. Lower-limb amputation; 5. Previous lower-limb bypass surgery or angioplasty. v. ≥1 risk factors: 1. BMI ≥ 27 kg/m2; 2. Dyslipidemia; 3. Family history (first degree relative: parents or siblings only) of coronary heart disease or stroke before the age of 60 years; 4. Hypertension; ...See full criteria on ClinicalTrials.gov Always talk to your doctor about whether this trial is right for you.

These are translations of the protocol\'s inclusion and exclusion criteria, simplified for patients and caregivers. The original clinical text appears below. Eligibility is ultimately confirmed by the trial site\'s screening process — this summary is a starting point for a conversation with your doctor, not a final determination.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: 1. Patients currently hospitalized or being discharged from hospital who have suffered an ACS, defined as follows: i. MI, defined by positive troponin T, troponin I, or CK-MB levels (as defined by institution-specific cut-offs) and ≥ 1 of the following: 1. Ischemic symptoms for ≥ 20 min; 2. Electrocardiogram (ECG) changes indicative of ischemia (ST-segment elevation or depression); 3. Development of pathological Q waves on the ECG ii. Unstable angina with significant coronary artery disease, defined by all of the following: 1. Ischemic symptoms for ≥ 20 min; 2. ECG changes indicative of ischemia (ST-segment changes); 3. At least one lesion ≥ 50% on angiogram performed during the current hospitalization. \[Note: patients who undergo cardiac catheterization or percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG) surgery will be eligible provided they are able to start varenicline in-hospital and nicotine e-cigarette at discharge.\] OR Outpatients with the following diagnoses/conditions: i. Cardiovascular: 1. Coronary artery disease documented with angiography or coronary CT; 2. Previous ACS, MI, stable or UA; 3. Previous coronary revascularization (e.g. PCI or CABG). ii. Renovascular: a. Chronic kidney disease. iii. Cerebrovascular: a. Previous cerebral infarction or transient cerebral ischemic attack. iv. Peripheral vascular: 1. Abdominal aortic aneurysm \> 3.0 cm or previous aortic aneurysm surgery; 2. Ankle-brachial pressure index of \< 0.9 or intermittent claudication; 3. Documented carotid artery disease; 4. Lower-limb amputation; 5. Previous lower-limb bypass surgery or angioplasty. v. ≥1 risk factors: 1. BMI ≥ 27 kg/m2; 2. Dyslipidemia; 3. Family history (first degree relative: parents or siblings only) of coronary heart disease or stroke before the age of 60 years; 4. Hypertension; 5. Males aged ≥ 55 years/females aged ≥ 60 years; 6. Diabetes mellitus. vi. Heart-related conditions: <!-- --> 1. Atrial fibrillation or flutter; 2. Cardiomyopathy; 3. Heart failure; 4. Left ventricular hypertrophy (evidenced by echocardiography or ECG); 5. Valvular disease (evidenced by echocardiography). 2. Smoked on average ≥ conventional cigarettes/day for the past year; 3. Age ≥18 years; 4. Motivated to quit smoking according to the Motivation To Stop Scale (MTSS) (≥ level 5); 5. Able to understand and provide informed consent in English or French; 6. If randomized to the combination arm (varenicline and e-cigarette plus counseling), willing and able to purchase e-cigarettes with the following properties: rechargeable, closed system that uses sealed cartridges or pods, tobacco or no flavor only, and nicotine strength of 20 mg/ml (2%) or less; 7. Likely to be available for 52 weeks of follow-up. Exclusion Criteria: 1. Pregnant or lactating females; 2. Use of any of the following in the 30 days prior to eligibility assessment: i. Varenicline or bupropion for smoking cessation; ii. Nicotine or non-nicotine e-cigarettes; iii. Other anti-craving medication (e.g., naltrexone, acamprosate) with the potential to alter substance-seeking behaviors; 3. Use of nicotine replacement therapy (NRT) in the 7 days prior to eligibility assessment \[Note: If participant is prescribed non-study NRT while hospitalized, they can continue using the non-study NRT until being discharged, even while taking the investigational products. Upon discharge, use of the non-study NRT should be stopped.\]; 4. Use of varenicline or e-cigarettes (nicotine or non-nicotine) for ≥14 days consecutively in the past year; 5. Previous serious adverse reaction to varenicline and/or e-cigarettes (nicotine or non-nicotine); 6. NYHA or Killip Class III or IV at the time of randomization; 7. Any unstable psychiatric disorder (as per enrolling physician); 8. Renal impairment with creatinine levels ≥2 times upper limit of normal or eGFR ≤15; 9. Use of any illegal drugs in the past year; 10. Planned use of cannabis (smoked) or other tobacco products (smoked or other) during the study period. \[Note: use of cannabis which is not smoked is permitted (e.g., edibles, ingested or vaped oils). However, methods which involve combustion could invalidate biochemical validation via exhaled carbon monoxide.\]

Treatments Being Tested

COMBINATION_PRODUCT

Combination Therapy Arm (Varenicline and Nicotine E-Cigarettes Plus Counseling)

Varenicline and nicotine e-cigarettes plus counseling

OTHER

Varenicline Plus Counseling

Varenicline plus counseling

Locations (13)

Trial sites listed on ClinicalTrials.gov for this study. Site activation status can vary — confirm with the specific site before traveling for a screening visit.

Fraser Clinical Trials
New Westminster, British Columbia, Canada
Dr. Georges-L.-Dumont University Hospital Center
Moncton, New Brunswick, Canada
NL Health Sciences
St. John's, Newfoundland and Labrador, Canada
Queen Elizabeth II Health Sciences Center
Halifax, Nova Scotia, Canada
St. Joseph's Hospital
London, Ontario, Canada
University of Ottawa Heart Institute
Ottawa, Ontario, Canada
Sunnybrook Health Sciences Centre
Toronto, Ontario, Canada
Montreal Heart Institute
Montreal, Quebec, Canada
Centre Hospitalier de L'Universite de Montreal
Montreal, Quebec, Canada
Montreal General Hospital
Montreal, Quebec, Canada
Jewish General Hospital
Montreal, Quebec, Canada
Institut Universitaire de Cardiologie et de Pneumologie de Québec
Québec, Quebec, Canada
Royal University Hospital
Saskatoon, Saskatchewan, Canada

How to Talk to Your Doctor About This Trial

Bring the printable summary of this trial — including the NCT ID (NCT05257629), the sponsor (Sir Mortimer B. Davis - Jewish General Hospital), and the key eligibility criteria — to your next appointment. Your doctor can review the inclusion and exclusion criteria against your medical history, lab values, and current treatments to assess whether you are likely to qualify. They can also help you weigh whether trial participation makes sense alongside your existing care plan.

Useful questions to walk through together: What does the trial protocol require beyond standard care? How long is the active treatment phase, and how long is follow-up? Are there study visits at sites I can reach? Who pays for the trial-specific procedures, and who pays for standard-of-care portions? See our 25 questions to ask about clinical trials guide for a more complete checklist.

Authoritative Sources

The official record for this trial lives on ClinicalTrials.gov — the federal registry maintained by the National Library of Medicine at NIH. For background on how this trial fits into the FDA approval pathway, see the FDA drug approval process. For oncology-specific guidance for patients considering trials, the National Cancer Institute publishes patient-oriented overviews. International trial registries are aggregated by the WHO ICTRP.

Frequently Asked Questions

What is the NCT05257629 clinical trial studying?

The ASAP Trial is a 5-year, multi-centre, randomized controlled trial that will assess the efficacy, safety, and tolerability of aggressive smoking cessation therapy among people at elevated cardiovascular risk. It will recruit 798 adult patients smoking on average at least 10 conventional (tobacco) cigarettes per day who are motivated to quit smoking and have either been diagnosed with ACS requiring hospitalization or are outpatients at elevated cardiovascular risk. Patients will be randomized (1:1) to one of two treatment arms: (1) combination therapy of varenicline and nicotine e-cigarettes… The full protocol is registered on ClinicalTrials.gov and includes the primary outcome measures, eligibility criteria, and study endpoints.

Who can participate in NCT05257629?

Eligibility for this trial depends on the specific inclusion and exclusion criteria set by the sponsor. The plain-English summary above translates the most important criteria into accessible language; the official clinical text is preserved in the collapsible section underneath. Whether you fit any specific trial is a medical decision your doctor needs to confirm — bring the trial information to your treating physician for a full review against your medical history.

How do I contact the trial site for NCT05257629?

Contact information registered with ClinicalTrials.gov is shown in the sidebar of this page. Before reaching out, confirm with your treating physician that this trial is appropriate for your situation. The trial site will then walk you through the screening process to determine final eligibility.

Is participating in a clinical trial safe?

Clinical trials in the United States are regulated by the FDA and overseen by Institutional Review Boards (IRBs) that review the protocol for safety. Risk varies by trial — Phase 1 studies test new treatments in humans for the first time, while Phase 3 trials use treatments that have already passed earlier safety screening. The informed consent document for any specific trial details the known risks and what to expect. Discuss those risks with your physician before deciding whether to participate.

Where can I verify the data on this page?

Every detail on this page comes directly from the ClinicalTrials.gov API. Click "View on ClinicalTrials.gov" in the sidebar to see the official, unmodified record. The federal record is always authoritative; this page is a structured presentation with a plain-English eligibility translation. For background on how clinical trials are regulated, see the FDA drug approval process documentation.

How This Page Is Built

Every field on this page is pulled directly from the ClinicalTrials.gov API v2 — no estimates, no proxies. The plain-English eligibility translation is generated from the original protocol text and reviewed for fidelity to the underlying clinical criteria. The original clinical text remains visible in the collapsible section above so users and clinicians can verify the translation. Read the full methodology for the data pipeline and known limitations.

Source: ClinicalTrials.gov API v2 record for NCT05257629. Maintained by the National Library of Medicine at NIH. Public domain. Cite as: "TrialFinderData. NCT05257629. Data: ClinicalTrials.gov."

Medical disclaimer: This page is informational, not medical advice. Talk to your doctor about whether a clinical trial is right for you.

Last updated 2026-05-08 · Data from ClinicalTrials.gov.