Clin2
NCT05100693Possibly a fitRecruiting

FETO balloon removal during pregnancy for diaphragm hernia

Congenital Diaphragmatic Hernia

Part of Genetic & congenital clinical trials.

This trial studies “smart removal” of a balloon placed in the womb to treat a baby’s congenital diaphragmatic hernia (CDH). It aims to see if removing the balloon in a planned, safer way can improve outcomes for the baby and keep mothers safe.

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

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

Who can take part

  • You are pregnant with a single baby diagnosed with an isolated congenital diaphragmatic hernia (CDH)
  • Your baby’s lung size on ultrasound must fit the trial’s severity ranges for left or right CDH
  • You must be at least 18 years old
  • You (or your legal representative) must sign consent before any screening and agree to post-birth ultrasound if needed
  • You must be able to stay close to UZ Leuven until the balloon is removed
  • You cannot have a latex allergy, leaking membranes (PROM), or any condition that makes the procedure unsafe
  • You cannot be enrolled in another interventional trial with an investigational drug or device

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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