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Early Assessment of Respiratory Function, Inflammation and Bronchial Reshuffle Among Newborns Screened for Cystic Fibrosis

Not Applicable
Completed
Conditions
Cystic Fibrosis
Registration Number
NCT02883816
Lead Sponsor
University Hospital, Montpellier
Brief Summary

The main objective of this study is to show that there is a concordance between lung disease at 13 months and the existing 9 weeks in newborn babies with cystic fibrosis asymptomatically.

This will identify at the first examination at 8 weeks, newborns who have the most impaired lung function at 13 months. To meet this objective an assessment of their lung function at 9 weeks and 1 month will be performed in newborns diagnosed with cystic fibrosis.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
52
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Change from respiratory function at 7 months and 11 months7 months and 11 months

measurement of lung volumes and flow rates of bronchial

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CHU Montpellier

🇫🇷

Montpellier, France

CHU Montpellier
🇫🇷Montpellier, France

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