Impact of CFTR-modulation with elexacaftor/tezacaftor/ivacaftor on the exercise capacity, intestinal and respiratory microbiome, microbial and inflammatory metabolites in cystic fibrosis
- Conditions
- E84.0Cystic fibrosis with pulmonary manifestations
- Registration Number
- DRKS00023862
- Lead Sponsor
- Zentrum für Kinder- und Jugendmedizin der Universitätsmedizin Mainz
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 84
Age 6 and older
- Confirmed diagnosis and mutation
- Planned to start medication with elexacaftor/tezacaftor/ivacaftor
- Written informed consent (from parent or legal guardian if underaged)
Or sex- and aged matched healthy control
- Comorbidity which exclude therapy with elexacaftor/tezacaftor/ivacaftor (e.g liver or renal insufficiency)
- Respiratory infection at the start of treatment
- Acute therapy changes 21 days before starting therapy with elexacaftor/tezacaftor/ivacaftor
- Antibiotic treatment up to 3 weeks prior to study start
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ongitudinal changes in diversity, species richness and in microbial composition of respiratory and intestinal microbiome and in exercise capacity (peak oxygen uptake and maximal work rate) during the therapy with CFTR-modulators.
- Secondary Outcome Measures
Name Time Method Secondary objectives include<br>- Evaluation of systemic inflammatory parameter (CRP, IgG, IL-8, TNF-alpha, TGF-beta), intestinal and airway inflammation (faecal calprotectin, Il-8 and NE in sputum) and urine cathepsine.<br>- Lung function measurement with spirometry and MBW will be performed to assess absolute changes in ppFEV1, ppFVC, ppFEV75-25 and in LCI.<br>- Changes in concentration of sweat chloride.<br>- Cystic Fibrosis Questionnaire-Revised (CFQ-R) will be completed at all visits.<br>- Assessment of CF metabolome by mass spectroscopy for CF-specific biomarkers.