Actively Recruiting
MPN Childhood Registry
Led by University of Erlangen-Nürnberg Medical School · Updated on 2026-05-01
500
Participants Needed
1
Research Sites
782 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Myeloproliferative neoplasms (MPNs) are caused by defects in blood cell production. This leads to an overproduction of mature cells, such as red blood cells or platelets. As a result, clinical symptoms and complications can develop. Circulatory disorders and resulting pain symptoms, such as headaches, are the most prominent. Furthermore, blood clotting disorders can occur, leading to vascular occlusions or bleeding. Over a longer period, bone marrow transformation into fibrous tissue or the development of acute leukemia can occur, resulting in even more serious complications. In the vast majority of cases, MPNs are diagnosed in older adults. These diagnoses are extremely rare in children and adolescents. Therefore, clinical and genetic characteristics, treatment options, and outcomes in pediatric patients with MPNs are insufficiently described, and only limited data are available for standardizing diagnostic and therapeutic approaches for MPNs in childhood and adolescence. Recommendations and guidelines from the adult field, which have largely been adopted and applied to children and adolescents, do not adequately address the specific needs of patients in childhood and adolescence. To gain more insights into MPN during this early, vulnerable phase of life, we have established a nationwide registry in Germany that systematically collects data from children and adolescents with MPN. The registry focuses particularly on the scientific analysis of the biological characteristics and differences of MPN in children and adolescents compared to adults.
CONDITIONS
Official Title
MPN Childhood Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Newly diagnosed polycythemia vera, essential thrombocythemia, primary myelofibrosis, or primary hypereosinophilic syndrome
- Age under 18 years (up to 17 years and 365 days) at diagnosis
- Patient treated in a participating center
- Written informed consent given for registry participation
You will not qualify if you...
- Secondary polycythemia, thrombocytosis, myelofibrosis, or hypereosinophilic syndrome caused by conditions other than polycythemia vera, essential thrombocythemia, primary myelofibrosis, or primary hypereosinophilic syndrome
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Pediatrics and Adolescent Medicine, University Hospital Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, Erlangen, Germany
Erlangen, Bavaria, Germany, D-91054
Actively Recruiting
Research Team
A
Axel Karow, PD Dr. med.
CONTACT
F
Franziska Fahrmeier, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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