Inflammatory and Microbiologic Markers in Sputum: Comparing Cystic Fibrosis With Primary Ciliary Dyskinesia

Mise à jour : Il y a 4 ans
Référence : NCT01155115

Femme et Homme

  • | Pays :
  • Canada
  • | Organes :
  • -
  • | Spécialités :
  • -

Extrait

The objective of this study is to compare the lower airways inflammatory response to infection/pulmonary exacerbation among children known to have Primary Ciliary Dyskinesia (PCD) with children known to have Cystic Fibrosis (CF) as measured by the presence of inflammatory mediators in expectorated/induced sputum.


Critère d'inclusion

  • Cystic fibrosis ,Primary Ciliary Dyskinesia

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