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Prevalence of Exercise-induced Ventilatory Limitation and Associated Factors in Patients With Cystic Fibrosis Receiving Elexacaftor-Tezacaftor-Ivacaftor

Prevalence of Exercise-induced Ventilatory Limitation and Associated Factors in Patients With Cystic Fibrosis Receiving Elexacaftor-Tezacaftor-Ivacaftor

Recruiting
18 years and older
All
Phase N/A

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Overview

Cystic fibrosis is a genetic disorder affecting the entire body and associated with respiratory exacerbations, impaired quality of life and reduced life expectancy. The therapeutic management of cystic fibrosis has been profoundly changed by the recent arrival of a combination of highly effective cystic fibrosis transmembrane conductance regulator (CFTR) modulators, Elexacaftor-Tezacaftor-Ivacaftor (ETI), which improve quality of life, respiratory function and reducing the number of exacerbations. The impact of these treatments on exercise adaptation has not been clearly identified.

The main objective is to estimate the prevalence of ventilatory reserve amputation during submaximal exercise testing assessed by the 6-minute walk test (6MWT) in patients with cystic fibrosis treated with ETIs.

Description

Cystic fibrosis is a genetic disorder affecting the entire body and associated with respiratory exacerbations, impaired quality of life and reduced life expectancy. The therapeutic management of cystic fibrosis has been profoundly changed by the recent arrival of a combination of highly effective cystic fibrosis transmembrane conductance regulator (CFTR) modulators, Elexacaftor-Tezacaftor-Ivacaftor (ETI), which improve quality of life, respiratory function and reducing the number of exacerbations. The impact of these treatments on exercise adaptation has not been clearly identified.

The main objective is to estimate the prevalence of ventilatory reserve amputation during submaximal exercise testing assessed by the 6-minute walk test (6MWT) in patients with cystic fibrosis treated with ETIs.

Eligibility

Inclusion Criteria:

  • Male or female
  • Adult aged 18 or over
  • Suffering from cystic fibrosis
  • Treated at the CRCM in Lille and Créteil
  • Treated by ETI
  • Be covered by social security
  • Be able to understand the requirements of the study, provide written informed consent, and comply with the study's data collection procedures

Exclusion Criteria:

  • Medical contraindication or inability to perform a stress test according to ERS recommendations
    • Absolute contraindications
    • Relative contraindications:
  • Exacerbation of the condition in the 4 weeks preceding the V1 visit (27).
  • Pregnant or breastfeeding women
  • Administrative reasons
  • Persons deprived of their liberty
  • Minors or protected adults
  • Persons who have refused or are unable to give informed consent
  • Persons in emergency situations

Study details
    Cystic Fibrosis (CF)
    Mucoviscidosis

NCT07314229

University Hospital, Lille

13 May 2026

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