European Registry for Myeloproliferative Neoplasms (MPNs) - Update of ERNEST Study

NCT ID: NCT04153305

Last Updated: 2023-01-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1010 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-10-08

Study Completion Date

2020-12-31

Brief Summary

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The Fondazione per la Ricerca Ospedale di Bergamo (FROM) decided to propose and promote the completion of ERNEST registry: the aim of the project is to obtain up-to-date estimates of clinical outcome of these patients in primary and secondary Myelofibrosis that have been included in the 'original' ERNEST study. The last was conducted between 2012 and beginning of 2015 including 1292 patients with Myelofibrosis, but it was interrupted in 2015 because of bankruptcy of the previous sponsor.

Detailed Description

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Follow-up of patients already been registered in the ERNEST registry resulting alive and/or in active surveillance at November 2014 (Blood 2014 124:1849) will be updated retrospectively until December 2020. Data collection will be centralized at Fondazione per la Ricerca Ospedale di Bergamo (FROM), and performed by a web-based and Electronic Data Capture (EDC) system through ad hoc electronic case report forms (e-CRFs). The e-CRFs system will be pre-filled with pre-existing data collected from cases already entered in the registry. Information on therapies received and outcome events occurred (in term of death, evolution to acute leukemia, secondary cancer and cardiovascular complications) until December 2020 will be recorded by authorized participating investigators.

Conditions

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Myelofibrosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* previous registration in the ERNEST registry (2012 - 2014)
* diagnosis of MF performed between January 2001 and 2012 December
* Signed informed consent to continue participation in the registry

Exclusion Criteria

None
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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FROM- Fondazione per la Ricerca Ospedale di Bergamo- ETS

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tiziano Barbui, MD

Role: STUDY_CHAIR

Fondazione per la Ricerca Ospedale di Bergamo

Locations

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AOU Careggi

Florence, FI, Italy

Site Status

UOC Ematologia, ASST Papa Giovanni XXIII

Bergamo, Lombardy, Italy

Site Status

Divisione Ematologia, Fondazione IRCCS Policlinico San Matteo

Pavia, Lombardy, Italy

Site Status

U.O. Ematologia, Ospedale di Circolo e Fondazione Macchi Varese

Varese, Lombardy, Italy

Site Status

Hospital ClĂ­nic de Barcelona

Barcelona, , Spain

Site Status

Center is Hematology Section, Uddevalla Hospital

Uddevalla, , Sweden

Site Status

Countries

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Italy Spain Sweden

Other Identifiers

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ERNEST - FROM/O1- 2019

Identifier Type: -

Identifier Source: org_study_id

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