North American Fetal Therapy Network Prospective Registry for Long-term Outcome Following Fetoscopic Endoluminal Tracheal Occlusion in Severe Left and Right Congenital Diaphragmatic Hernia

Key facts

Sponsor

Mayo Clinic

Principal Investigator

Mauro Schenone, MD, M.D

Mayo Clinic

Intervention

Fetoscopic Endoluminal Tracheal Occlusion(device)

Enrollment

80 target

Eligibility

18-50 years · FEMALE

Timeline

2026 – 2038

Study locations (1)

• Mayo Clinic in Rochester, Rochester, Minnesota, 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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• RECRUITINGNANCT05354505
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• RECRUITINGPHASE4NCT05213676
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• RECRUITINGPHASE3NCT07187206
  Safety and Efficacy of FETO in CDH Phase III
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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
  The University of Texas Health Science Center, Houston
• RECRUITINGNANCT03138863
  Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia (FETO)
  Rodrigo Ruano

See all trials for Congenital diaphragmatic hernia →