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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
PTGS1 Genetic Variation and Increased Risk for Persistent Pulmonary Hypertension of the NewbornCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Infant, Newborn, Diseases, lung disorder, persistent fetal circulation syndrome, pulmonary hypertension, respiratory system disorderRecruitingNot stated2026-01-26NCT00710177

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OrganizationsLinked trials
Medical College of Wisconsin201

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Research sitesCityCountryLinked trials
Children's WisconsinMilwaukeeUnited States23