Cystic Fibrosis Clinical Trials

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

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
France
University Hospital
RECRUITING
Lille
Contact Information
Primary
Camille AUDOUSSET, Doctor
DRC@chu-lille.fr
+33 3.20.44.41.45
Time Frame
Start Date: 2025-12-17
Estimated Completion Date: 2027-04-04
Participants
Target number of participants: 130
Treatments
Experimental: patients treated with ETI (Kaftrio-Kalydeco©)
Related Therapeutic Areas
Sponsors
Collaborators: Vaincre la Mucoviscidose
Leads: University Hospital, Lille

This content was sourced from clinicaltrials.gov