Clin2
NCT00106015Possibly a fitRecruiting

Diamond Blackfan Anemia Registry Study

AnemiaBlood Disease

Part of Blood & lymphatic clinical trials.

This study collects information from patients with Diamond Blackfan Anemia (DBA), a rare blood disorder that affects red blood cell production. By joining this registry, you help doctors better understand DBA and improve treatments for patients like you.

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

Phase
N/A
Enrollment
900 people
Ages
Any age
Study type
Observational

Who can take part

  • You have been diagnosed with Diamond Blackfan Anemia based on blood tests showing low red blood cells with few immature red cells in your bone marrow
  • You do not have another bone marrow failure syndrome such as Fanconi anemia, dyskeratosis congenita, or Shwachman Diamond syndrome
  • Your diagnosis is confirmed either by typical blood and bone marrow findings or by genetic testing showing a DBA gene mutation

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.

Similar studies

Other trials that look related to this one.

NCT06250595Recruiting
European rare blood disorder registry

This study is building a registry of people with rare blood diseases. By joining, you help doctors learn more about these conditions and improve future care.

Barcelona, Catalonia
NCT07186179Recruiting
Stem cell mobilization for diamond blackfan anemia

This trial tests whether a medication can help move your own blood stem cells from your bone marrow into your bloodstream, so they can be collected. This is a first step toward possibly using those cells in a future treatment for diamond blackfan anemia.

New Hyde Park, New York
NCT02442011Recruiting
Blood disorder biosample study

This trial collects and studies blood samples from people with blood disorders. It may help researchers better understand blood conditions using lab testing rather than a new medication.

The Bronx, New York
NCT06056908Recruiting
Shwachman Diamond Syndrome Registry and Study

This study is creating a registry for people with Shwachman-Diamond Syndrome (SDS) or similar conditions, and their family members. It aims to learn more about the condition and improve care by collecting health information over time.

Aurora, Colorado
NCT02720679Recruiting
Study genetics behind blood disorders in children and families

This study looks at genetic (DNA) factors that may contribute to certain blood disorders. You may be invited if you or a close family member is receiving care for a blood condition like MDS or MPN, and the study also includes related relatives.

Memphis, Tennessee
NCT02964494Recruiting
Congenital anemia registry for congenital dyserythropoietic anemia

This study is a registry that collects medical and lab information from people with congenital dyserythropoietic anemia (CDA), a lifelong type of anemia that can cause jaundice. It helps doctors better understand the condition and its causes, including in families where it runs.

Cincinnati, Ohio

Hear when a new Anemia trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.