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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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11 March 2024 |
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Main ID: |
NCT03527004 |
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Date of registration:
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04/05/2018 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Cross-Sectional Survey on the Use of Tobacco Products - Italy
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Scientific title:
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Cross Sectional Survey on the Use of Tobacco Products in the General Population and in Users of IQOS in Italy (2018-2020) |
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Date of first enrolment:
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March 20, 2018 |
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Target sample size:
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6107 |
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Recruitment status: |
Terminated |
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URL:
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https://clinicaltrials.gov/ct2/show/NCT03527004 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Switzerland
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Contacts
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Name:
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Pierpaolo Magnani |
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Address:
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Telephone:
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Email:
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Affiliation:
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Philip Morris Products S.A. |
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Key inclusion & exclusion criteria
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Inclusion Criteria (all participants, including IQOS users):
- Legally permitted to buy tobacco products in Italy (=18 years of age).
- Currently residing in Italy.
- Able to read, write and understand Italian.
- Consent to participate in the survey
Inclusion Criteria (IQOS users only):
- Has used more than 100 HEETS tobacco sticks in his or her lifetime.
- Is currently using IQOS.
- Has access to the internet.
- Is not currently employed by Philip Morris International or any of its affiliates
Exclusion Criteria:
- Not meeting the inclusion criteria.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Tobacco Use
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Intervention(s)
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Other: Survey on Use of Tobacco Products in the General Population
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Other: Survey on Use of Tobacco Products in IQOS Users
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Primary Outcome(s)
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Prevalence of current tobacco use
[Time Frame: Study duration (3 years).]
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IQOS use experience
[Time Frame: Study duration (3 years).]
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Past tobacco use status
[Time Frame: Study duration (3 years).]
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Perceived risk
[Time Frame: Study duration (3 years).]
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Self-reported health status
[Time Frame: Study duration (3 years).]
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Secondary ID(s)
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P1-PMX-02-IT
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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