SWITCH: Effects of Switching From Cigarettes to Tobacco Heating System on Coronary Atherosclerosis Progression

Sponsor
Institute of Cardiology, Warsaw, Poland (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05660798
Collaborator
PMPSA (Other)
180
1
2
35.9
5

Study Details

Study Description

Brief Summary

Objective:

To evaluate the impact of heated versus combustion tobacco products on progression of atherosclerosis in patients with CAD unable(unwilling) to quit smoking.

Rationale:

Despite the efforts to curb smoking and full awareness of its deleterious health impact, smoking remains a significant contributor to morbidity and mortality. Some health impact of smoking may be improved by other forms of cigarettes than traditional combustion, especially for subjects unwilling or unable to stop smoking. As recently as 2020, one of heated tobacco products (HTP)(IQOS) was FDA Authorized as a 'Reduced Exposure' product. The available evidence to date allows to conclude that the IQOS system heats tobacco but does not burn it, which significantly reduces the production of harmful and potentially harmful chemicals. Scientific studies have shown that switching completely from conventional cigarettes to the IQOS system significantly reduced body's exposure to harmful or potentially harmful chemicals. There is also evidence indicating lower levels of inflammatory markers and improved vascular function associated with use of heated tobacco products. However, it is unknown whether the reduction in the exposure translates into potential reduction of harm within cardiovascular system, as compared to the traditional (combustion) cigarettes.

The evidence is of crucial importance for patients with cardiovascular diseases, medical community, and national health authorities planning evidence based policies regarding HTP/cigarettes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: heated tobacco - lifestyle intervention
N/A

Detailed Description

Objective:

To evaluate the impact of heated versus combustion tobacco products on progression of atherosclerosis in patients with CAD unable(unwilling) to quit smoking.

Background Despite the efforts to curb smoking and full awareness of its deleterious health impact, smoking remains a significant contributor to morbidity and mortality. Some health impact of smoking may be improved by other forms of cigarettes than traditional combustion, especially for subjects unwilling or unable to stop smoking. As recently as 2020, one of heated tobacco products (HTP)(IQOS) was FDA Authorized as a 'Reduced Exposure' product. The available evidence to date allows to conclude that the IQOS system heats tobacco but does not burn it, which significantly reduces the production of harmful and potentially harmful chemicals. Scientific studies have shown that switching completely from conventional cigarettes to the IQOS system significantly reduced body's exposure to harmful or potentially harmful chemicals. There is also evidence indicating lower levels of inflammatory markers and improved vascular function associated with use of heated tobacco products. However, it is unknown whether the reduction in the exposure translates into potential reduction of harm within cardiovascular system, as compared to the traditional (combustion) cigarettes.

The evidence is of crucial importance for patients with cardiovascular diseases, medical community, and national health authorities planning evidence based policies regarding HTP/cigarettes.

Methods:

Prospective, single-centre, open-label, randomised study including 180 stable patients with coronary artery disease (CAD) as diagnosed on CCTA, without indications for invasive treatment, unable(unwilling) to quit smoking, randomised 1:1 to either heated (group H) or combustion (group C) tobacco products and followed for 18 months. The follow-up is accomplished with CCTA scan. The study clinical visits are planned at 1, 3, 6, 12, and 18 months.

The primary outcome is change in non calcified plaque volume at 18 months between H and C groups (intention to treat design).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
180 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Effects of Switching From Cigarettes to Tobacco Heating System on Coronary Atherosclerosis Progression in Patients With Stable Coronary Artery Disease
Anticipated Study Start Date :
Jan 2, 2023
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2025

Arms and Interventions

Arm Intervention/Treatment
No Intervention: combustion tobacco

Experimental: heated tobacco

Behavioral: heated tobacco - lifestyle intervention
Patients unable (unwilling) to stop smoking will be randomized to either combustion (C) or heated (H) tobacco groups.

Outcome Measures

Primary Outcome Measures

  1. Change in non calcified plaque volume between H and C groups ("intention to treat") [0-18 months]

    CCTA based evaluation

Secondary Outcome Measures

  1. Change in total plaque volume [0-18 months]

    CCTA based evaluation

  2. Change in plaque volume components (low attenuation, fibrous-fatty, fibrous, non-calcified plaque, calcified plaque) [0-18 months]

    CCTA based evaluation

  3. Change in non calcified plaque volume between H and C groups ("as treated") [0-18 months]

    CCTA based evaluation

  4. Change in lipid metabolism [0-18 months]

    Total cholesterol (TC) Triglycerides (TG) Lipoproteins: low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) Apolipoproteins: apolipoprotein A1 (ApoA1), apolipoprotein B (ApoB) Lipoprotein(a) Lp(a)

  5. Change in oxidative stress [0-18 months]

    8-Epi prostaglandin F2 alpha (8 epi PGF2α) Myeloperoxidase (MPO)

  6. Change in inflammation [0-18 months]

    High-sensitivity C-reactive protein (hs CRP) White blood cell (WBC) counts Homocysteine Interleukins (IL-6) Fibrinogen

  7. Change in platelet activation [0-18 months]

    11-dehydro-thromboxane B2 (11 DTX B2) Plasminogen activator inhibitor-1 (PAI-1) Tissue plasminogen activator (t-PA) Platelet count Mean platelet volume (MPV)

  8. Change in endothelial dysfunction [0-18 months]

    P-selectin Metalloproteinase 9 (MMP-9)

  9. Change in haemodynamic stress [0-18 months]

    N-terminal pro b-type natriuretic peptide (NT-proBNP)

  10. Change in myocardial injury [0-18 months]

    high-sensitivity troponin T (hs-TnT)

  11. Change in glycemia control [0-18 months]

    Fasting Blood Glucose, HbA1c

  12. Change in physical activity [0-18 months]

    self reported, mobile device monitoring

  13. Change in exposure to nicotine [0-18 months]

    4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol , Nicotine equivalents in spot urine , 2-cyanoethylmercapturic acid

  14. SAFETY (ADVERSE OUTCOMES) [0-18 months]

    Independent DSMB will evaluate the outcomes

  15. Change in self reported product use [0-18 months]

  16. Change in quality of life [0-18 months]

    EQ5D-5L

  17. Cost/effectiveness analysis [0-18 months]

  18. Subgroup analysis (AGE/SEX/CO-MORBIDITIES) [1-18 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Adults aged >18 years and <75 years

  2. Subjects with stable chronic coronary syndrome defined as the presence of at least one coronary artery stenosis >=20% due to coronary plaque visible on coronary computed tomography angiography (CCTA), in an artery with a reference diameter > 2.0mm

  3. History of smoking pack-years ≥10 (Pack-years will be calculated by taking the average number of cigarettes smoked per day divided by 20 and multiplied by the number of years smoked), based on self-reporting

  4. Current smokers with a minimum of self-reported current smoking pattern of >10 cigarettes/day during the last 6 months prior to screening, smoking status will be verified based on a urinary cotinine test (cotinine ≥200 ng/mL)

  5. Patients that have been advised to quit smoking and informed of a smoking risk and cessation programs (per local SOC) and who are still not willing to set a quit date within the next 30 days at screening

  6. Stable treatment for coronary atherosclerosis according to the guidelines

  7. Have understood the study and have signed informed consent

Exclusion Criteria:
  1. Any acute cardiovascular event (i.e. ACS, MI, Stroke, TIA, Limb ischemia), unstable angina or revascularization within 30 days prior to screening

  2. Planned coronary intervention (PCI, CABG) at screening

  3. Previous CABG

  4. Preexisting heart failure with reduced ejection fraction (EF <50%)

  5. Severe uncontrolled hypertension (at the discretion of investigator)

  6. Diabetes

  7. Subjects with documented genetic familial hypercholesterolemia

  8. Subjects have known serious infection or chronic inflammatory systemic disease (e.g. rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis)

  9. Subjects have a known non-cardiovascular disease that is associated with poor prognosis (e.g. metastatic cancer)

  10. Patient with currently active cancer or history of cancer within the last 5 years

  11. Subjects have hypersensitivity or any other warnings listed in the local labeling for THS

  12. Subjects have hypersensitivity to imaging iodine contrast agents

  13. GFR<45 ml/min/1,73 m2

  14. Subjects who could not participate for any reason other than medical (e.g., psychological and/or social reason) per Investigator's judgment

  15. Subjects have any other clinical condition that would jeopardize the subject's safety while participating in this study, per Investigator's judgment

  16. Female subject is pregnant or breast-feeding, or planning to become pregnant during the study

  17. Subjects have previously participated in this study, or in an interventional study (drug or medical device) within 30 days of screening (participation in observational studies/registries allowed)

  18. Subjects have a close affiliation with the investigational site: a close relative of the investigator, a person dependent on the investigational site (e.g. employee or student of the investigational site)

  19. Subjects are current or former employee of the tobacco industry or their first-degree relatives (parent, child, spouse)

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Institute of Cardiology Warsaw Poland 04-628

Sponsors and Collaborators

  • Institute of Cardiology, Warsaw, Poland
  • PMPSA

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Institute of Cardiology, Warsaw, Poland
ClinicalTrials.gov Identifier:
NCT05660798
Other Study ID Numbers:
  • SWITCH01
First Posted:
Dec 21, 2022
Last Update Posted:
Dec 28, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 28, 2022