Recruiting
Phase 3

ASAP

Sponsor:

Sir Mortimer B. Davis - Jewish General Hospital

Code:

NCT05257629

Conditions

Acute Coronary Syndrome

Cardiovascular Diseases

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

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

Varenicline Plus Counseling

Study Details

Brief summary:

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.

Conditions

Acute Coronary Syndrome

Cardiovascular Diseases

Study ID

NCT05257629

Start date

Feb 2, 2023

Status verified date

Apr, 2025

Completion date

Mar 7, 2027

Anticipated

Primary completion date

Mar 7, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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. \[Note: use of cannabis which is not smoked is permitted (e.g., edibles, ingested or vaped oils). However, methods which involve combustion could invalidate biochemical validation via exhaled carbon monoxide.\]

Study Design

Enrollment

798 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

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

Patients in the combination therapy arm will be supplied funds and instructions for the purchase of e-cigarettes and cartridges/pods upon hospital discharge and at the week 4 and 12 clinic visits. As with standard NRTs such as the gum, inhaler, and lozenge, the investigators expect smokers will self-regulate administration according to their withdrawal symptoms. Use will be monitored via self-report for telephone follow-ups. At clinic visits, patients will be asked to bring their e-cigarettes, used and unused cartridges/pods, and purchasing receipts. Patients will be advised regarding the signs and symptoms of nicotine toxicity and of an allergic reaction.

other: Varenicline Plus Counseling

All patients will begin varenicline in-hospital upon randomization. For the first 3 days, patients will take a 0.5 mg tablet once a day. They will then take a 0.5 mg tablet twice a day for the following 4 days, and one 1 mg tablet twice a day from day 8 onward for the remainder of the 12-week treatment. Use will be monitored via self-report for telephone follow-ups and return of all unused tablets at the end of the treatment period. Should a patient experience severe side effects (such as headache, nausea, vomiting, dizziness, dyspepsia, fatigue, insomnia, abnormal dreams, constipation, or flatulence) on day 8 onward, the varenicline dose should be reduced from 1 mg twice daily to 0.5 mg twice daily prior to study medication discontinuation.

Interventions

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

Varenicline and nicotine e-cigarettes plus counseling

Varenicline Plus Counseling

Varenicline plus counseling

Primary outcome measure

  • Number of participants with 7-day point prevalence smoking abstinence [ Time Frame: 24 weeks ]

Central Contacts and Locations

Locations

Fraser Clinical Trials

Recruiting

New Westminster, British Columbia, Canada, V3L 3W4

Contacts

Principal Investigator:

Sina Alipour

Dr. Georges-L.-Dumont University Hospital Center

Recruiting

Moncton, New Brunswick, Canada, E1C 2Z3

Contacts

Principal Investigator:

Jean-Francois Baril

NL Health Sciences

Recruiting

Saint John's, Newfoundland and Labrador, Canada, A1B 3V6

Contacts

Principal Investigator:

Mohammad Almutawa

Queen Elizabeth II Health Sciences Center

Recruiting

Halifax, Nova Scotia, Canada, B3H 3A7

Contacts

Principal Investigator:

Jafna Cox

St. Joseph's Hospital

Recruiting

London, Ontario, Canada

Contacts

Principal Investigator:

Neville Suskin

University of Ottawa Heart Institute

Recruiting

Ottawa, Ontario, Canada, K1Y 4W7

Contacts

Principal Investigator:

Hassan Mir

Sunnybrook Health Sciences Centre

Recruiting

Toronto, Ontario, Canada, M4N 3M5

Contacts

Principal Investigator:

Eugene Crystal

Montreal General Hospital

Recruiting

Montreal, Quebec, Canada, H3G 1A4

Contacts

Principal Investigator:

Thao Huynh

Jewish General Hospital

Recruiting

Montreal, Quebec, Canada, H3T 1E2

Contacts

Principal Investigator:

Mark Eisenberg

Montreal Heart Institute

Recruiting

Montréal, Quebec, Canada, H1T 1C8

Contacts

Principal Investigator:

Jean-Francois Tanguay

Centre Hospitalier de L'Universite de Montreal

Recruiting

Montréal, Quebec, Canada, H2X 3E4

Contacts

Principal Investigator:

Stephane Elkouri

Institut Universitaire de Cardiologie et de Pneumologie de Québec

Recruiting

Quebec City, Quebec, Canada, G1V 4G5

Contacts

Principal Investigator:

Tomas Cieza

Royal University Hospital

Recruiting

Saskatoon, Saskatchewan, Canada, S7N 0W8

Contacts

Rama Mangipudi

rkm352@mail.usask.ca

Principal Investigator:

Jay Shavadia

More Information

Sponsor

Sir Mortimer B. Davis - Jewish General Hospital

Last update posted

Apr 29, 2025

Last verified

Apr, 2025

Keywords

  • acute coronary syndrome
  • smoking cessation
  • randomized controlled trial
  • varenicline
  • e-cigarettes
  • cardiovascular disease

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Sir Mortimer B. Davis - Jewish General Hospital on 2025-04-29.