← Eichor
Study identifier: NCT05797272 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

In-utero Hematopoietic Stem Cell Transplantation for the Treatment of Fetuses With Bart's Hydrops Fetalis Syndrome

Condition: Haemoglobin Barts Hydrops  ·  Sponsor: Chinese University of Hong Kong

PhaseNA
Planned participants10
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective observational pilot study on pregnant women who are diagnosed to have Bart's hydrops fetalis syndrome (BHFS) affected fetuses and opt for continuation of pregnancy will be invited to consider undergoing in-utero hematopoietic stem cell transplantation under a research protocol, aiming to determine whether in-utero hematopoietic stem cell transplantation (HSCT) for fetuses with confirmed BHFS at the time of in-utero transfusion (IUT) of red blood cells could be feasible in Hong Kong. The participants will undergo bone marrow or peripheral blood stem cells harvest and an IUT combined with maternal stem cells.

This description comes directly from the study's public registry record.

Talk to the study team

Tak Yeung LEUNG, MD  ·  852-35052806  ·  tyleung@cuhk.edu.hk

Always discuss trial participation with your own doctor first.

Locations (1)

The Chinese University of Hong KongShatin, Hong KongRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05797272