COVID-19 Epidemic and Patients With Myeloproliferative Neoplasias
NCT ID: NCT04416438
Last Updated: 2022-10-18
Study Results
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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COMPLETED
1793 participants
OBSERVATIONAL
2020-05-18
2022-09-01
Brief Summary
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Detailed Description
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This is an exploratory descriptive study in order to put in place as soon as possible a possible strategy for the protection of patients most at risk.
The study will include all consecutive patients with MNP according to the WHO (World Health Organization) classification seen in consultation or teleconsultation over the duration of the study, whether or not they have had a COVID-19 infection.
The collection of clinical data, treatment regimens and survival and death data will be carried out by the investigator or a member of his medical team, after delivering an information note to the patient informing him of the computerized processing of his data, subject to the patient's non-objection.
The diagnosis of asymptomatic COVID 19 will be made on the presence of a positive serology and on the absence of clinical signs on questioning.
The presence of a symptomatic COVID 19 infection will be posed on the presence of clinical signs +/- CT as identified by the practitioner who treated the patient and confirmed or not by a positive PCR and / or a positive serology.
Data collected:
* Socio-demographic data (gender, date of birth)
* Description of hemopathy and its treatment
* Description of COVID-19 infection and its management
* Biological data: blood count, specific COVID-19 test results if available (PCR, serology).
* History, comorbidities
* Evolution of COVID-19 infection and possible specific treatment
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Seen in consultation or teleconsultation from May 2020 or deceased if the investigator became aware of this death during the study period
Exclusion Criteria
18 Years
ALL
No
Sponsors
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French Intergroup of Myeloproliferative syndromes
UNKNOWN
French Innovative Leukemia Organisation
OTHER
Responsible Party
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Principal Investigators
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Jean-Jacques KILADJIAN, Pr
Role: PRINCIPAL_INVESTIGATOR
FIM
Laurence LEGROS, Dr
Role: PRINCIPAL_INVESTIGATOR
FIM
Locations
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Paris Saint Louis
Paris, , France
Countries
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Other Identifiers
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COVIM
Identifier Type: -
Identifier Source: org_study_id
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