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RecruitingNCT06250595ENROLUpdated Feb 9, 2024

European Rare Blood Disorders Platform (ENROL)

An observational study in Anemia, Bone Marrow Failure and Bleeding Disorder, sponsored by Hospital Universitari Vall d'Hebron Research Institute. Recruiting at 1 site in Spain. Open to participants aged Up to 100 Years. Per ClinicalTrials.gov, last updated 2024-02-09.

Sponsored by Hospital Universitari Vall d'Hebron Research Institute · Observational

From the registry’s dates

  • Started Jul 2022; still recruiting 4 years 4 months later.
Study type
Observational
Model
Case-control
Time perspective
Other
Enrollment
37,090
Ages
Up to 100 Years
Sex
All
01

Study summary

ENROL, the European Rare Blood Disorders Platform has been conceived in the core of ERN-EuroBloodNet as an umbrella for both new and already existing registries on Rare Hematological Diseases (RHDs). ENROL aims at avoiding fragmentation of data by promoting the standards for patient registries' interoperability released by the EU RD platform.

ENROL's principle is to maximize public benefit from data on RHDs opened up through the platform with the only restriction needed to guarantee patient rights and confidentiality, in agreement with EU regulations for cross-border sharing of personal data.

Accordingly, ENROL will map the EU-level demographics, survival rates, diagnosis methods, genetic information, main clinical manifestations, and treatments in order to obtain epidemiological figures and identify trial cohorts for basic and clinical research. To this aim, ENROL will connect and facilitate the upgrading of existing RHD registries, while promoting the building of new ones when / where lacking. Target-driven actions will be carried out in collaboration with EURORDIS for educating patients and families about the benefits of enrolment in such registries, including different cultural and linguistic strategies.

The standardized collection and monitoring of disease-specific healthcare outcomes through the ENROL user-friendly platform will determine how specialized care is delivered, where are the gaps in diagnosis, care, or treatment and where best to allocate financial, technical, or human resources.

Moreover, it will allow for promoting research, especially for those issues that remain unanswered or sub-optimally addressed by the scientific community; furthermore, it will allow promoting clinical trials for new drugs. ENROL will enable the generation of evidence for better healthcare for RHD patients in the EU as the ultimate goal.

ENROL officially started on 1st June 2020 with a duration of 36 months. ENROL is co-funded by the Health Programme of the European Union under the call for proposals HP-PJ-2019 on Rare disease registries for the European Reference Networks. GA number 947670

Read the detailed description

Study Title:

European Rare Blood Disorders Platform (ENROL)

Study Objectives:

The European Rare Blood Disorders Platform (ENROL) is conceived in the core of the European Reference Network on Rare Hematological Diseases (ERN-EuroBloodNet), as the umbrella platform for both new and already existing registries on Rare Hematological Diseases (RHDs) avoiding fragmentation of data by promoting the interoperability standards for patient registries.

ENROL aims at mapping demographics, diagnosis methods, genetic data, main clinical manifestations and treatments at the EU level by enabling the connection, upgrading and building of EU patients registries in line with EU data protection and interoperability standards with the following major objectives:

Promoting research: allowing the identification of patient cohorts to facilitate the development of collaborative projects on basic and clinical research on RHD Epidemiological surveillance: pooling of available data on registries and databases across European countries to monitor trends and provide essential epidemiologic information on RHD while enabling the generation of evidence for the optimum allocation of resources and health planning For this, ENROL will obtain comparable EU data for RHD on demographics, survival rates, diagnosis methods, genetic information, main clinical manifestations and treatments by promoting the interoperability standards for patient registries in line with the European Platform on Rare Disease Registration (EU RD Platform). ENROL is officially endorsed by the European Hematology Association (EHA).

Methodology:

Data on patients with RHDs will be collected retrospectively and prospectively at the time of inclusion on the registry and at 12-month intervals for all registered patients.

The ENROL strategy for data gathering combines the exhaustiveness of data collection at EU level for health planning and epidemiological purposes, with a higher level of RHD data granularity for promoting research and identification of patients' cohorts.

Accordingly, the platform has been designed to integrate data from any available sources, including Healthcare providers (ERN-EuroBloodNet members / Other EU healthcare providers) and EU/national/local existing registries. Data entry is also allowed with different levels of granularity to pursue ENROL aims, including counts/aggregated level data to increase data exhaustiveness at the EU level required for the epidemiological surveillance, and pseudonymised individual level data to promote research and facilitate the identification of trial groups.

As defined in GDPR Art. 26, a Joint Controllership is being established where the institutions conforming the Consortium (HUVH/VHIR, ULB/ERASME, CING and AP-HP) for the jointly determine the purposes and means of processing and assume equal responsibilities in terms of data protection.

Data processing and analyses will be conducted in various sub studies, after every 1000 patients included in the European Registry and/or at the end of each interim follow-up period (every 12 months).

Disease coverage

The study population consist of both males and females aged from 0 to 100 year old diagnosed as RHD according to ORPHANET classification (ORPHA 97992), including myeloid and lymphoid tumors (ORPHA 68347), rare anaemia disorders (ORPHA 108997), rare coagulation disorders (ORPHA 98429), and polycythemia (ORPHA 98427), and further complemented with rare hereditary hemochromatosis (ORPHA220489), included in the disease scope of ERN-EuroBloodNet following a request from well-established patient groups and experts.

Accordingly, ENROL disease coverage results in more than 450 different entities with differential clinical and etiological features i.e. oncological vs non-oncological, hereditary vs acquired, or significant difference frequency, among others, which can be classified into the following disease groups:

RAD: Inherited Rare Anaemia Disorders, including inherited Bone Marrow Failures BMF: Acquired Bone Marrow Failures Bleeding: Rare bleeding-coagulation disorders and related diseases HH-Iron: Hemochromatosis and other rare genetic disorders of iron metabolism and heme synthesis Myeloid: Myeloid malignancies Lymphoid: Lymphoid malignancies

ENROL dataset has been conceived in a bottom-up design for ensuring the capture of the common elements for rare diseases in line with the EU recommendations and with the EU RD platform, and the key features common for the whole spectrum for RHDs. Furthermore, the latest level can be stepped up for the definition of domain specific elements that support the in-depth analysis.

In the spirit of ENROL aims to promote the connection and linkage of available data sources and the creation of new registries where lacking. ENROL promotes collaborations for supporting the a) upgrade the existing registries and b) create new European registries in compliance with the standards of interoperability and ENROL policy. Collaboration agreements will be in place for the transfer of a subset of the data elements gathered to ENROL.

Study Duration and funding

An extensive recruitment period and follow-up, as well as geographical coverage, is desirable for long-term sustainability of the European Epidemiological Platform. Accordingly, ENROL has not an expected ending date but continue the pooling and processing of data for an indeterminate period of time.

ENROL is co-funded by the Health Programme of the European Union under the call for proposals HP-PJ-2019 on Rare disease registries for the European Reference Networks. GA number 947670.

02

Conditions studied

  • Anemia
  • Bone Marrow Failure
  • Bleeding Disorder
  • Iron Metabolism Disorders
  • Myeloma
  • Lymphoid Neoplasm
  • Myeloma, Malignant
  • Leukemia
  • Anemia, Sickle Cell
  • Thalassemia
  • Blood Cancer
  • Red Cell Membrane and Enzyme Abnormalities

Keywords

  • Anemia
  • Bone Marrow Failure
  • Bleeding disorder
  • Iron metabolism disorder
  • Myeloid
  • Lymphoid
  • Blood cancer
  • Leukemia
  • Red Cell membrane and Enzyme Abnormalities
  • Thalassemia
  • Sickle Cell Disease
03

In context

Anemia

1,810 studies on the registry are indexed under Anemia; 215 are open to participants now.

This study's planned enrollment of 37,090 is above the median of 270 across 368 observational studies indexed under Anemia.

Browse Anemia studies →

Lead sponsor

Hospital Universitari Vall d'Hebron Research Institute is the lead sponsor of 276 studies on the registry; 64 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Up to 100 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

Patients with Rare Hematological Disease

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients must meet all of the following criteria to be included in the ENROL Registry
  • Age from 0-100, both female and male
  • Diagnosed as RHDs according to ORPHANET classification
  • Able and willing to provide written (patient or legal representative for minors) if needed according to national legislation.

Exclusion criteria

Exclusion Criteria:

  • Patients diagnosed as traits or trait conditions for other recessive RHDs
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-control
Time perspective
Other
Enrollment
37,090 participants (estimated)
Target follow-up
15 Years
Patient registry
Yes

Groups and cohorts

  • Inherited Rare Anaemia Disorders, including inherited Bone Marrow Failures

    Patients with Inherited Rare Anemia Disorders, including inherited Bone Marrow Failures, stratified by gender, age, and/or variants/types if applicable.

    Other: Collection of clinical and laboratory data from EHR.

  • Acquired Bone Marrow Failures

    Patients with Acquired Bone Marrow Failures, stratified by gender, age, and/or variants/types if applicable.

    Other: Collection of clinical and laboratory data from EHR.

  • Rare bleeding-coagulation disorders and related diseases

    Patients with Rare bleeding-coagulation disorders and related diseases, stratified by gender, age, and/or variants/types if applicable.

    Other: Collection of clinical and laboratory data from EHR.

  • Hemochromatosis and other rare genetic disorders of iron metabolism and heme synthesis

    Patients with hemochromatosis and other rare genetic disorders of iron metabolism and heme synthesis, stratified by gender, age, and/or variants/types if applicable.

    Other: Collection of clinical and laboratory data from EHR.

  • Myeloid malignancies

    Patients with Myeloid malignancies, stratified by gender, age, and/or variants/types if applicable.

    Other: Collection of clinical and laboratory data from EHR.

  • Lymphoid malignancies

    Patients with lymphoid malignancies, stratified by gender, age, and/or variants/types if applicable.

    Other: Collection of clinical and laboratory data from EHR.

Interventions

  • OtherCollection of clinical and laboratory data from EHR.

    Observational sutdy

06

What researchers measure

Primary outcomes

  1. Demography and epidemiology

    To collect and to describe demographics and epidemiological data of any type of RHDs.

    Time frame: 15 years

07

Study locations

1 of 1 sites recruiting
  • María del Mar
    Barcelona, Catalunya 08035, Spain
    Recruiting
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2022 (actual). Primary completion is estimated for Jul 2037, 180 months after the start.

Of 124 non-industry observational studies under Anemia, half reached primary completion within 30 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 84. This study's planned 180 months is above that.

Counting every sponsor, half of 145 studies reached it within 30 months; a quarter within 12 and three quarters within 76.

How these figures are worked out, and which studies are left out of them.

Registered
Dec 4, 2023
First posted
Feb 9, 2024
StartActual
Jul 1, 2022
Primary completionEst.
Jul 2037
CompletionEst.
Jul 2037
Last update
Feb 9, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 9, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06250595
Collaborators
ERN-EuroBloodNet (European Reference Network on Rare Hematological Diseases
Responsible party
Sponsor
First posted
Feb 9, 2024
Start date
Jul 1, 2022
Primary completion
Jul 2037 (estimated)
Completion
Jul 2037 (estimated)
Last update
Feb 9, 2024

Study contacts

María del Mar Manú Pereira, PhD
Contact
mar.manu@vhir.org
+34934893000
Victoria Gutiérrez Valle, Biotech
Contact
victoria.gutierrez@vhir.org
+34934893000
María del Mar Manú Pereira, PhD
principal investigator · Vall d'Hebron Institut de Recerca / University Hospital Vall d'Hebron (VHIR / HUVH)
Béatrice Gulbis, MD
principal investigator · Hôpital ERASME / ULB (ERASME_ULB)
Petros Kountouris, PhD
principal investigator · Cyprus Institute of Neurology and Genetics (CING)
Pierre Fenaux, MD
principal investigator · Assistance Publique - Hopitaux de Paris (AP-HP)

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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