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NCT04026360: SCILD

Impact of Early Lung Physiology, Viral Infections and the Microbiota on the Development and Progression of Lung Disease in Children With Cystic Fibrosis

Recruiting now Last updated 4 November 2020
What this trial tests

trial testing no intervention in Confirmed Diagnosis of Cystic Fibrosis in 500 participants. Currently enrolling.

Timeline
1 July 2011
Primary endpoint
31 August 2050
31 December 2050

Quick facts

Lead sponsorInsel Gruppe AG, University Hospital Bern
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment500
Start date1 July 2011
Primary completion31 August 2050
Estimated completion31 December 2050
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Insel Gruppe AG, University Hospital Bern

Who can join

Adults 0 to 18, any sex, with Confirmed Diagnosis of Cystic Fibrosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study collects data on microbiological factors and lung function parameters (e.g. spirometry, body plethysmography, lung-MRI) to assess their interaction on the lung growth and lung development of infants and children with Cystic Fibrosis (CF).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Hyperinflation is associated with increased respiratory rate and is a more sensitive measure of cystic fibrosis lung disease during infancy compared to forced expiratory measures.
    Muston HN, Slaven JE, Tiller C, Clem C, et al · · 2021 · cited 4× · PMID 34143539 · DOI 10.1002/ppul.25538

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Other trials of no intervention

Trials testing the same drug.

Other Insel Gruppe AG, University Hospital Bern trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04026360.

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