MPN Childhood Registry
NCT07410247 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500
Last updated 2026-05-01
Summary
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
- Childhood Myeloproliferative Neoplasms
Interventions
- OTHER
-
Observation
Observation
Sponsors & Collaborators
-
University of Erlangen-Nürnberg Medical School
lead OTHER
Principal Investigators
-
Axel Karow, MD · Department of Pediatrics and Adolescent Medicine, University Hospital Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, Erlangen, Germany
Eligibility
- Min Age
- 0 Years
- Max Age
- 17 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-01-01
- Primary Completion
- 2032-12-31
- Completion
- 2037-12-31
Countries
- Germany
Study Locations
More Related Trials
-
Magnetic Resonance Imaging in Treating Children With Progressive Low-Grade Astrocytoma
NCT00005084 ·Status: UNKNOWN ·Phase: PHASE2
-
Observation of Young Patients Who Are Undergoing Surgery for Craniopharyngioma
NCT00258453 ·Status: COMPLETED ·Phase: NA
-
Nimotuzumab in Children With Intrinsic Pontine Glioma
NCT00561691 ·Status: COMPLETED
-
Integrated PET/MRI and Germline Variants to Differentiate Brain Tumopr Recurrence From Iatrogenicchanges in Children
NCT06226519 ·Status: RECRUITING
-
Natural History With Focus on Oncological Risk Evaluation in Pediatric Patients With PTEN Pathogenic Variants
NCT06805734 ·Status: RECRUITING
-
Morphological Analysis of the Pineal Gland in Pediatric Retinoblastoma Patients Using Magnetic Resonance Imaging
NCT01884194 ·Status: COMPLETED
-
Multicenter Register for Children and Young Adults With Intracranial Localized Medulloblastoma, CNS-PNET or Ependymoma
NCT02238899 ·Status: COMPLETED
-
Psychosocial Situation of Children With Rare Solid Abdominal Tumors and Their Families
NCT05245123 ·Status: COMPLETED
-
Mechanism of Action of Interferon in the Treatment of Myeloproliferative Neoplasms
NCT05850273 ·Status: RECRUITING
-
Memory Neuroimaging in Children, Adolescents and Young Adults Following Pediatric Cancer
NCT04324450 ·Status: COMPLETED ·Phase: NA
-
International Rare Brain Tumor Registry
NCT05697874 ·Status: RECRUITING
-
Establishment and Clinical Application of Risk Classification Model Based on Molecular Typing of Medulloblastoma in Children
NCT05406947 ·Status: NOT_YET_RECRUITING
-
Functional and Structural Outcomes Following Childhood Bone or Soft Tissue Sarcomas of the Lower Extremity
NCT06737172 ·Status: ACTIVE_NOT_RECRUITING
-
Rare Embryonal Tumors of the Central Nervous System: International Registry
NCT05711992 ·Status: RECRUITING
-
Genetic and Molecular Risk Profiles of Pediatric Malignant Brain Tumors in China
NCT05672043 ·Status: RECRUITING
-
Radiation Induced Alterations in Resting State Brain Networks in Pediatric Brain Tumor Patients
NCT06185686 ·Status: RECRUITING
-
Molecular Analysis of Samples From Patients With Diffuse Intrinsic Pontine Glioma and Brainstem Glioma
NCT01106794 ·Status: RECRUITING
-
Multicenter Registry for Patients With Childhood.Onset Craniopharyngioma, Xanthogranuloma, Cysts of Rathke's Pouch, Meningioma, Pituitary Adenoma, Arachnoid Cysts
NCT04158284 ·Status: RECRUITING
-
Study of Stored Tumor Samples in Young Patients With Brain Tumors
NCT00897286 ·Status: TERMINATED
-
An International Clinical Program for the Diagnosis and Treatment of Children With Ependymoma
NCT02265770 ·Status: RECRUITING ·Phase: PHASE2/PHASE3
-
Study of Brain Tumors (Tectal Tumors) Using Magnetic Resonance Imaging
NCT00229814 ·Status: WITHDRAWN
-
Multi-parametric Biomarker Development to Predict Malignant Conversion in Patients With Neurofibromatosis Type 1
NCT05677594 ·Status: ACTIVE_NOT_RECRUITING
-
International Diffuse Intrinsic Pontine Glioma (DIPG)/Diffuse Midline Glioma (DMG) Registry and Repository
NCT03101813 ·Status: RECRUITING
-
Proton Beam Radiation Therapy in Treating Young Patients Who Have Undergone Biopsy or Surgery for Medulloblastoma or Pineoblastoma
NCT00105560 ·Status: COMPLETED ·Phase: NA
-
A Study of How Proton Beam Radiotherapy (PBRT) Affects Brain Function and Quality of Life in Children and Young Adults Undergoing Treatment for a Brain Tumor
NCT05288439 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA