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European Exposure Study

P

Philip Morris

Status

Completed

Conditions

Smoking

Study type

Observational

Funder types

Industry

Identifiers

NCT01237912
SPA0403

Details and patient eligibility

About

The current study was designed to determine the exposure of adult smokers and non-smokers to cigarette smoke constituents through evaluation of selected biomarkers of exposure.

Full description

The purpose of the study was to provide a greater knowledge about human exposure to cigarette smoke constituents by evaluating selected biomarkers of exposure in smokers and non-smokers. This was an observational, parallel-group study to be conducted at multiple centres in the UK, Germany, and Switzerland. It was planned to enrol sufficient subjects such that at least 1440 subjects complete the study.

Enrollment

1,667 patients

Sex

All

Ages

21 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Smokers: Subjects who smoked commercial cigarettes exclusively (less than or equal to 10 mg ISO tar yield in Germany and the UK; less than or equal to 12 mg ISO tar yield in Switzerland) with a regular consumption of at least 1 cigarette per day over the last 12 months without change in brand over the previous 3 months.

or

Non-smokers: Subjects who did not smoke commercial cigarettes, hand-rolled cigarettes, cigars, pipes, bidis, and did not use other nicotine-containing products (patch, gum, lozenges etc.) within 1 year prior to Visit 1 and throughout the study duration.

Exclusion criteria

  • Female subjects with child-bearing potential were to be excluded if

    1. Subject was pregnant (or did not have negative pregnancy tests) or breast-feeding
    2. Subject did not agree to use an acceptable method of contraception

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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