Clinical Trial

Safety and Efficacy of Fetoscopic Endoluminal Tracheal Occlusion (FETO) in Congenital Diaphragmatic Hernia (CDH)

Recruiting
View on ClinicalTrials.gov →
Summary
The purpose of the study is to determine if babies with left or right-sided CDH that undergo the FETO procedure survive more often and have fewer long-term complications than babies that have similar left or right-sided CDH that elect not to have the FETO procedure performed during pregnancy.
Protocol Amendment History 3 changes
notable Primary completion pushed: 2030-04 -> 2036-04 2026-06-30
minor Completion pushed: 2031-04 -> 2038-04 2026-06-30
critical Recruitment opened 2026-06-02
Trial Details
NCT Number NCT07577414
Lead Sponsor Dr Erin Perrone
Conditions Congenital Diaphragmatic Hernia
Enrollment 40 participants
Start Date 2026-06-17
Primary Completion 2036-04 (estimated)
Study Completion 2038-04 (estimated)
Updated on ClinicalTrials.gov 2026-06-29