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RADeep Multicenter European Epidemiological Platform for Patients Diagnosed With Rare Anemia Disorders (RADs)

Recruiting
Conditions
Sideroblastic Anemia
Hereditary Anemia
Sickle Cell Disease
Constitutional Aplastic Anemia
Iron Metabolism Disorders
Anemia Due to Membrane Defect
CDA
Thalassemia
Hemolytic; Anemia, Hereditary, Due to Enzyme Disorder
Interventions
Other: Data collection from EHR.
Registration Number
NCT06213402
Lead Sponsor
Hospital Universitari Vall d'Hebron Research Institute
Brief Summary

Rare Anaemia Disorders (RADs) is a group of rare diseases characterized for presenting anaemia as the main clinical manifestation. Different medical entities classified as RADs by ORPHA classification are most of them chronic life threating disorders with many unmet needs for their proper clinical management creating an impact on European health systems. RADs present diagnostic challenges and their appropriate management requires from specialised multidisciplinary teams in Centers of expertise.

Although there are some examples of well-established national registries on RADs in EU, the lack of recommendations for Rare disease registries implementation and the lack of standards for interoperability has led to the fragmentation or unavailability of data on prevalence, survival, main clinical manifestations or treatments in most of the European countries.

Detailed Description

The Rare Anaemia Disorders European Epidemiological Platform (RADeep) is an initiative endorsed by the European Reference Network on Rare Hematological Diseases (ERN-EuroBloodNet) under the frame of the European Blood Disorders Platform (ENROL), the ERN-EuroBloodNet umbrella platform officially endorsed by the European Hematology Association (EHA) for European patients' registries on rare haematological diseases. RADeep will share pseudonymised level data with ENROL.

RADeep supports the standardized collection of data of patients affected by any RADs at the European level, maximizing public benefit from data on RADs opened-up with the only restriction needed to guarantee patient rights and confidentiality, in agreement with the General Data Protection Regulation and applicable laws for cross-border sharing of personal data. RADeep has the following major objectives:

1. To collect and describe the demographics, disease-management, and treatment outcomes of patients diagnosed with RADs

2. To perform observational studies concerning research questions and to present outcomes in the fields of health related to organ damage and risk stratification for identification of trial cohorts for new drugs and/or development of research projects

3. To promote harmonization and best practices in the prevention, diagnosis, treatment and follow-up of RADs patients by the dissemination of reliable Guidelines and the translation of research results into clinical practice.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
32564
Inclusion Criteria
  • Patients must meet all of the following criteria to be included in the RADeep Registry
  • Age from 0-100, both female and male
  • Diagnosed as RADs (SCD, THAL, PKD, and other RADs THAL according to ORPHANET classification)
  • Able and willing to provide written informed consent (patient or legal representative for minors)
Exclusion Criteria
  • Patient or legal representative for minors unwilling or unable to give consent
  • Patients diagnosed with SCD or THAL (alpha-thalassaemia and beta-thalassaemia) traits or trait conditions for other recessive RADs

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Sickle cell anaemia and other related sickle diseasesData collection from EHR.Patients with sickle cell disease and related diseases in current regular follow-ups in European-Union health centers
Thalassemia and related diseasesData collection from EHR.Patients with Thalassemia disease and related diseases in current regular follow-ups in European-Union health centers, stratified by age, gender, and/or variants/type if applicable.
Pyruvate Kinase Deficiency and related diseasesData collection from EHR.Patients with Pyruvate Kinase Deficiency and related diseases in current regular follow-ups in European-Union health centers, stratified by age, gender, and/or variants/type if applicable.
Red Blood Cell membrane disorders and related diseasesData collection from EHR.Patients with Reb Blood Cell membrane disorders and related diseases in current regular follow-ups in European-Union health centers, stratified by age, gender, and/or variants/type if applicable.
Primary Outcome Measures
NameTimeMethod
Estimation of Prevalence and Incidence of RADs15 years

Demography and epidemiology

To collect and to describe demographics and epidemiological data of any type of RADs:

* Estimate the population frequency of each RAD disease group and disease survival

* Estimate the diagnosis delay

* Identify cohorts of patients for research/clinical trials

* Estimate disease severity

* Assess the use of specific treatments

Descriptive analyses will be undertaken at the end of the follow-up period using standard statistical methods to examine the subjects' demographics, disease characteristics and management. Data is updated yearly in an electronic CRF form while assuring homogenization in categorization and units.

Time-to-event analyses, namely Kaplan-Meier and Cox proportional hazard regression will be used to estimate overall survival.

Multivariate Cox proportional hazards regression models will be used to identify variables that are important to correlate survival.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Vall d'hebron Research Institute - Vall d'Hebron Research Institute - University Hospital Vall d'Hebrón (VHIR/HUVH)

🇪🇸

Barcelona, Catalunya, Spain

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