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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Epididymis Protein 4 and Pulmonary Function With Quality Improvement Protocol Among Cystic Fibrosis PatientsCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Infant, Newborn, Diseases, cystic fibrosis, hereditary disease, lung disorder, pancreas disorder, respiratory system disorderRecruitingNot stated2025-04-08NCT06915961

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OrganizationsLinked trials
Ain Shams University347

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Research sitesCityCountryLinked trials
Ain Shams UniversityCairoEgypt2