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Recruiting NCT07342920

Study of the Prevalence of Active/Passive Smoking and Vaping Among Patients With Cystic Fibrosis

Observational Cystic Fibrosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Cystic Fibrosis. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

In the collective unconscious, a patient with cystic fibrosis does not smoke. This belief is so deeply rooted that there is virtually no French data on the prevalence of smoking among this vulnerable population. Faced with a cohort of patients undergoing a complete transformation (improved quality of life and life expectancy, fewer hospitalizations, reduced respiratory symptoms, better social integration), it is becoming urgent to assess the current situation in order to optimize tobacco prevention. This is all the more important given the emergence of international studies objectively examining the interactions between smoking, vaping, and the efficacy of Kaftrio.

Primary outcome measures

  • Prevalence of smoking in adults with cystic fibrosis [Time frame: Up to 12 months]

Eligibility criteria

Inclusion criteria

  • Adult patient (≥ 18 years old)
  • With confirmed cystic fibrosis
  • Regular follow-up at the Strasbourg Adult Cystic Fibrosis Center

Exclusion criteria

  • Patients who have undergone a double lung transplant for cystic fibrosis.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

France · 1 center
  • Service de Pneumologie - CHU de Strasbourg - France — Strasbourg

Identifiers

NCT: NCT07342920 · 9813

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗