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

Last updated: January 9, 2024
Sponsor: Hospital Universitari Vall d'Hebron Research Institute
Overall Status: Active - Recruiting

Phase

N/A

Condition

Red Blood Cell Disorders

Platelet Disorders

Nephropathy

Treatment

Data collection from EHR.

Clinical Study ID

NCT06213402
PR(AMI)427/2021
  • Ages < 100
  • All Genders

Study 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.

Eligibility Criteria

Inclusion

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 ORPHANETclassification)
  • Able and willing to provide written informed consent (patient or legal representativefor minors)

Exclusion

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) traitsor trait conditions for other recessive RADs

Study Design

Total Participants: 32564
Treatment Group(s): 1
Primary Treatment: Data collection from EHR.
Phase:
Study Start date:
November 30, 2021
Estimated Completion Date:
November 30, 2036

Study 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.

Connect with a study center

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

    Barcelona, Catalunya 08035
    Spain

    Active - Recruiting

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