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AnemiaENROLNCT06250595

European Rare Blood Disorders Platform (ENROL)

An observational study of Anemia and Bone Marrow Failure, run by Hospital Universitari Vall d'Hebron Research Institute at 1 site in Spain.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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). Read more about this study

Who is it for?
Ages Up to 100 years
Conditions the study is for
Anemia, Bone Marrow Failure, Bleeding Disorder
What is being tested?
Collection of clinical and laboratory data from EHR.
How many people
37,090 participants
Where
1 siteSpain
Study dates
1 Jul 2022to Jul 2037
How long will I take part?
15 Years
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Up to 100 years
  • All sexes
  • Child, Adult, Older adult

Study population: Patients with Rare Hematological Disease

Who may be able to join

  • 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 informed consent (patient or legal representative for minors) if needed according to national legislation.

Who cannot join

  • Patients diagnosed as traits or trait conditions for other recessive RHDs

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

María del Mar Manú Pereira, PhD contact

+34934893000

mar.manu@vhir.org

Victoria Gutiérrez Valle, Biotech contact

+34934893000

victoria.gutierrez@vhir.org

Spain1 site, 1 recruiting
  • María del Mar

    Barcelona, Catalonia, 08035

    María del Mar Mañú Pereira, Biologist, 0034934893000, mar.manu@vhir.org

    Victoria Gutiérrez Valle, Biotech, +34934893000, victoria.gutierrez@vhir.org

    Recruiting

Other trials in Spain

About this study

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.

Read more

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.

Being tested
Collection of clinical and laboratory data from EHR.
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
Medical subject headings
Anemia, Bone Marrow Failure Disorders, Hemostatic Disorders, Iron Metabolism Disorders, Neoplasms, Plasma Cell, Leukemia, Anemia, Sickle Cell, Thalassemia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Collection of clinical and laboratory data from EHR.Other

    Observational sutdy

Study groups in NCT06250595
Study groupRoleWhat they receive
Inherited Rare Anaemia Disorders, including inherited Bone Marrow FailuresPatients with Inherited Rare Anemia Disorders, including inherited Bone Marrow Failures, stratified by gender, age, and/or variants/types if applicable.
Receives: Other: Collection of clinical and laboratory data from EHR.
Acquired Bone Marrow FailuresPatients with Acquired Bone Marrow Failures, stratified by gender, age, and/or variants/types if applicable.
Receives: Other: Collection of clinical and laboratory data from EHR.
Rare bleeding-coagulation disorders and related diseasesPatients with Rare bleeding-coagulation disorders and related diseases, stratified by gender, age, and/or variants/types if applicable.
Receives: Other: Collection of clinical and laboratory data from EHR.
Hemochromatosis and other rare genetic disorders of iron metabolism and heme synthesisPatients with hemochromatosis and other rare genetic disorders of iron metabolism and heme synthesis, stratified by gender, age, and/or variants/types if applicable.
Receives: Other: Collection of clinical and laboratory data from EHR.
Myeloid malignanciesPatients with Myeloid malignancies, stratified by gender, age, and/or variants/types if applicable.
Receives: Other: Collection of clinical and laboratory data from EHR.
Lymphoid malignanciesPatients with lymphoid malignancies, stratified by gender, age, and/or variants/types if applicable.
Receives: Other: Collection of clinical and laboratory data from EHR.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Demography and epidemiology

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

    Measured: 15 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Feb 2024
  2. Study start1 Jul 2022
  3. Primary completionJul 2037 (estimated)
  4. Study completionJul 2037 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Other
Enrolment
37,090 participants (estimated)
Target duration
15 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT06250595
Sponsor's protocol ID
PR(AMI)294/2022
Acronym
ENROL
Status last verified
Dec 2023
First submitted
4 Dec 2023
Last updated
9 Feb 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Anemia and Bone Marrow Failure, run by Hospital Universitari Vall d'Hebron Research Institute at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 9 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact María del Mar Manú Pereira, PhD (+34934893000, mar.manu@vhir.org), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Demography and epidemiology (time frame: 15 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Feb 2024.

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