Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) for CDH
Start Date
9/1/2015
Completion Date
8/1/2030
Summary
The rationale for fetal therapy in severe congenital diaphragmatic hernia (CDH) is to restore adequate lung growth for neonatal survival.
Detailed Description
Prenatal tracheal occlusion (TO) obstructs the normal egress of lung fluid during pulmonary development leading to increased lung tissue stretch, increased cell proliferation, and accelerated lung growth. European colleagues have developed foregut endoscopy and techniques to position and remove endoluminal tracheal balloons in utero. Recently, the Belgium group published summary results of FETO showing an improved survival in 175 patients with isolated left CDH from 24% to 49%. The goal of this pilot study is to study the feasibility of implementing FETO therapy in the most severe group of fetuses with left CDH Observed/expected lung-to-head ratio \< 25%(O/E LHR \< 25%).
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Fetoscopic Endoluminal Tracheal Occlusion (FETO)
Conditions
Locations
Connecticut Children's Medical Center
Hartford, Connecticut 06106
United States