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Study identifier: NCT07166172 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prospective Registry for Long-term Outcomes Following FETO in Severe Left and Right CDH

Condition: Congenital Diaphragmatic Hernia · Congenital Abnormalities · Neonatal Diseases and Abnormalities  ·  Sponsor: Johns Hopkins University

PhaseNA
Planned participants80
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This registry study aims to confirm that FETO increases neonatal survival to discharge and reduces long-term morbidity in fetuses with isolated left CDH and o/e LHR \< 30%, or isolated right CDH and o/e LHR ≤ 45%, compared to those receiving standard care. This prospective registry plans to enroll 80 pregnant women (40 treatment/40 control) with fetuses diagnosed with isolated CDH, and the children will be followed for up to 24 months.

This description comes directly from the study's public registry record.

Talk to the study team

Ahmet Baschat, MD  ·  410-502-6561  ·  abascha1@jhmi.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Johns Hopkins HospitalBaltimore, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07166172