Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) for CDH

Key facts

Sponsor

Connecticut Children's Medical Center

Principal Investigator

Timothy Crombleholme, MD, M.D

Connecticut Children's Medical Center

Intervention

Fetoscopic Endoluminal Tracheal Occlusion (FETO)(device)

Enrollment

15 enrolled

Eligibility

18 years · FEMALE

Timeline

2015 – 2030

Study locations (1)

• Connecticut Children's Medical Center, Hartford, Connecticut, United States

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.

Other trials for Congenital diaphragmatic hernia

Additional recruiting or active studies for the same condition.

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• RECRUITINGPHASE3NCT07187206
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• RECRUITINGNANCT07166172
  Prospective Registry for Long-term Outcomes Following FETO in Severe Left and Right CDH
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• RECRUITINGNANCT06884423
  Safety and Efficacy of FETO in CDH: A Phase III Trial
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• RECRUITINGNANCT06739356
  North American Fetal Therapy Network for Long-term Outcome Following Fetoscopic Endoluminal Tracheal Occlusion in Severe Left and Right Congenital Diaphragmatic Hernia
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• RECRUITINGNANCT03138863
  Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia (FETO)
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See all trials for Congenital diaphragmatic hernia →