Clin2
NCT05771688Worth exploringRecruiting

Balloon procedure for severe left lung birth defect

Hernia, DIaphragmatic, Congenital

Part of Genetic & congenital, Injuries & trauma clinical trials.

This trial studies a fetal procedure where doctors place a small balloon to help a severe left-sided lung birth defect (CDH) develop better. It aims to improve baby outcomes by temporarily blocking the airway in the womb, starting in a specific week range of pregnancy.

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

  • You are pregnant and carrying one baby (not twins or more).
  • The baby’s birth defect is left-sided CDH, not right-sided or both sides.
  • Your ultrasound shows severe CDH with an O/E LHR under 25%.
  • Genetic testing must not show a harmful change (microarray) and chromosome testing must not show major problems; no known lethal birth defects besides CDH.
  • You must be between 27 weeks 0 days and 29 weeks 6 days when the balloon would be placed, and your cervix must measure more than 20 mm.
  • You must be able to stay very close to the hospital during the balloon period (within 15 minutes) with enough family/caregiver help, and you must be willing to sign consent.

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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