Clin2
NCT05797272Worth exploringRecruiting

In-utero stem cell treatment for Bart’s hydrops

Haemoglobin Barts Hydrops

Part of Blood & lymphatic, Genetic & congenital, Immune system & allergy, Women’s health & pregnancy clinical trials.

This trial studies whether giving hematopoietic (blood-forming) stem cells while the baby is still in the womb can treat fetuses with Bart’s hydrops fetalis syndrome. It aims to improve outcomes after prenatal intervention in carefully selected pregnancies.

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 before 26 weeks and have a confirmed diagnosis of Bart’s hydrops fetalis syndrome (BHFS) from a prenatal test (CVS, amniocentesis, or cordocentesis).
  • You and the parents choose to move forward with in-utero treatment and are willing to continue it for the rest of the pregnancy if needed.
  • The fetus does not have a second major birth defect (not related to BHFS) that would make outcomes much worse.
  • The fetus does not have other major genetic or chromosome problems besides BHFS that would make outcomes much worse.
  • Ultrasound or heart (echocardiogram) checks do not show a very high risk that the baby will die after the procedure.
  • The pregnancy has not ended in loss (in-utero death) before the treatment happens.

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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