Clin2
NCT05354505Possibly a fitRecruiting

Balloon procedure in pregnancy for severe diaphragmatic hernia

Diaphragmatic Hernia

Part of Genetic & congenital clinical trials.

This trial studies a prenatal procedure called FETO, where a small balloon is placed in the fetal windpipe to help lung growth in babies with a severe diaphragmatic hernia. It may improve newborn outcomes by preparing the lungs before birth.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
10 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Be pregnant, age 18 or older, with one baby (singleton pregnancy)
  • Agree to sign consent and follow all study visits and procedures for the pregnancy
  • Have a clear genetic test (normal microarray/karyotype); if late in pregnancy, some other accepted tests may work
  • The baby must have diaphragmatic hernia with very severe underdeveloped lungs (based on LHR and liver position) and a fetal heart ultrasound with no major heart defects
  • Be able to travel and stay near NewYork-Presbyterian/Columbia (within 30 minutes) and attend frequent follow-ups
  • You must not have certain medical risks (for example, specific allergies, preterm-cervix issues, placenta problems, some infections, or not being safe for the procedure)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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