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

Key facts

Sponsor

Johns Hopkins University

Principal Investigator

Ahmet Baschat, MD, M.D

Johns Hopkins University

Intervention

Fetal Treatment Arm (FETO Group)(device)

Enrollment

80 enrolled

Eligibility

18 years · FEMALE

Timeline

2025 – 2031

Study locations (1)

• Johns Hopkins Hospital, Baltimore, Maryland, United States

Collaborators

KARL STORZ Endoscopy-America, Inc.

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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