Skip to content

Evaluation of the Lung Clearance Index

Evaluation of Lung Clearance Index for Early Detection of Lung Disease in Young Children With Cystic Fibrosis

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02342951
Acronym
LCI
Enrollment
53
Registered
2015-01-21
Start date
2014-04-01
Completion date
2019-07-01
Last updated
2026-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cystic Fibrosis

Keywords

Cystic fibrosis,, lung clearance index,, pulmonary function

Brief summary

The purpose of this study is to determine the efficacy of a non invasive method of detecting the pulmonary disease in order to initiate treatment against cystic fibrosis as soon as possible. Moreover this screening procedure permits to note the improvement following the treatment and to choose the optimal treatment in term of efficacy.

Detailed description

It is mandatory to detect as early as possible lung CF disease in the young child with CF to initiate active therapies limiting irreversible lesions. Lung Clearance Index (LCI) which evaluates gas clearance from the alveolar volume is an easy to-do technique in pre-school children. Main objective To evaluate correlation between LCI and thoracic low dose computed tomodensitometry (CT) endpoints at initial visit Secondary objectives 1. To evaluate correlation between LCI and respiratory function measurements at each visit 2. To evaluate correlation between the evolution of LCI and respiratory function endpoints and the evolution of CT only for the children for whom a thoracic low dose CT is requested by their referent doctor after two years. 3. To evaluate LCI predictive value for respiratory function 2 years later in preschool children. This is a prospective multicenter cohort study. Study visits will be performed each year during the annual check up for normal follow up of the child. Initial visit (Visit 1) takes place during an annual check-up during which a low dose CT was prescribed. It will include following tests: LCI, Lung function tests (LFTs) performed according to age (forced volumes and flows, plethysmographic specific airway resistances and interrupter resistances), and a low dose CT scan performed according a standardized protocol. Visit 2 will be performed 12 ± 3 months later and will include following tests: LCI , LFTs. Visit 3 will be performed 24 ± 3 months later and will include following tests: LCI , LFTs and, if judged necessary by the child's referent doctor, a low dose CT scan performed according to a standardized protocol. Anthropometric data, infection history, treatment will be collected at each visit. Recruiting period: 1 year Study period: 2 years per patient, 3 years as a whole LCI will help to evaluate early ventilation inhomogeneity due to small bronchi abnormalities in young children with CF. Concordance between LCI and CT endpoints evaluation will help to define the frequency of lung CT administration in young CF children. Predictive value for later abnormal lung function development will be evaluated. This will help to detect the children at risk to develop abnormal lung function and to target those requiring active treatment. Finally this endpoint will be very valuable in the future therapeutic trials for CFTR correctors or potentiators.

Interventions

OTHERLung clearance index determination

Lung clearance index determination

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER
Vaincre la Mucoviscidose
CollaboratorOTHER
URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to 6 Years
Healthy volunteers
No

Inclusion criteria

* Children with typical cystic fibrosis (sweat chloride level \>60 mEq/l) followed in reference centre participating to the study * From 3 to 6 years old * Children with a planned annual assessment that required thoracic computed tomography and lung function test * Children with informed and non opposed parents

Exclusion criteria

* Children with atypical cystic fibrosis * Children with bronchial exacerbation dating less than 2 weeks * Children with severe associated disease

Design outcomes

Primary

MeasureTime frame
measure of nitrogen washout and Brody 2 scoreMonth 0

Secondary

MeasureTime frameDescription
measure of FEV (Correlation between the evolution of LCI and respiratory function endpoints and CT)2 yearsCorrelation between the evolution of LCI and respiratory function endpoints and CT
measure of FEV (Evaluation of LCI predictive value for respiratory function in preschool children)2 yearsEvaluation of LCI predictive value for respiratory function in preschool children.

Countries

France

Contacts

PRINCIPAL_INVESTIGATORMuriel Le Bourgeois, MD

Service de pneumologie pédiatrique, Hôpital Necker-Enfants Malades Assistance Publique Hôpitaux de Paris 75015 Paris, France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026