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CompletedNCT04422470CHRONOS19Updated Jan 26, 2023

Registry of Patients With Hematologic Disease and COVID-19 in Russia

An observational study in Coronavirus Infection and Hematologic Diseases, sponsored by National Research Center for Hematology, Russia. Completed at 15 sites in Russian Federation. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-01-26.

Sponsored by National Research Center for Hematology, Russia · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
666
Ages
18 Years and older
Sex
All
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Study summary

This is an observational prospective cohort study to evaluate the clinical course and outcomes of COVID-19 and the underlying disease in patients with hematologic disease (malignant or non-malignant).

Read the detailed description

This is a web-based registry. After registration, physicians from hematology clinical centers and hospitals in Russia will receive access to the web platform for clinical trial management to fill in the online data collection form in a de-identified manner. This form includes questions about general clinical history of hematologic disease, manifestation, treatment, and the course of COVID-19, concomitant conditions, consequences on the hematologic disease, short-term and long-term outcomes. It will take approximately 10 min to answer the questions. Patients will be followed for 30 days after COVID-19 diagnosis and up to 6 months for hematologic disease outcomes and overall survival assessment.

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Conditions studied

  • Coronavirus Infection and Hematologic Diseases

Keywords

  • COVID-19
  • Blood diseases
  • Leukemia
  • Lymphoma
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In context

COVID-19

7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.

This study's enrollment of 666 is above the median of 261 across 3,136 observational studies indexed under COVID-19.

Browse COVID-19 studies →

Lead sponsor

National Research Center for Hematology, Russia is the lead sponsor of 21 studies on the registry; 6 are open to participants now.

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

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with hematologic disease (both malignant and non-malignant) infected with SARS-CoV-2

Inclusion criteria

  • Age 18 or older
  • Any previously or currently diagnosed hematologic disease
  • Laboratory confirmed or suspected (based on clinical symptoms and/or CT) COVID-19
  • Known outcome of COVID-19 in case of retrospective data input (protocol allows retrospective data input for patients who were prospectively followed in local centers)

Exclusion criteria

Exclusion Criteria

  • Loss of follow-up within 30 days after COVID-19 diagnosis
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
666 participants (actual)
Target follow-up
6 Months
Patient registry
Yes

Interventions

  • OtherNon-interventional study

    Non-interventional study

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What researchers measure

Primary outcomes

  1. 30-day all-cause mortality

    Rate of death from any cause

    Time frame: 30 day

Secondary outcomes

  1. COVID-19 complications

    Rate of COVID-19 complications

    Time frame: 30 day

  2. ICU admission

    Rate of ICU admission

    Time frame: 30 day

  3. Mechanical ventilation / O2 requirement

    Rate of mechanical ventilation / O2 requirement

    Time frame: 30 day

  4. Relapse or progression of hematologic disease

    Rate of relapse or progression of hematologic disease

    Time frame: 30 day, 90 day and 180 day

  5. Overall survival

    Number of patients alive

    Time frame: 30 day, 90 day and 180 day

  6. Risk factors

    Putative risk factors for the severity and lethality of COVID-19

    Time frame: 30 day, 90 day and 180 day

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Study locations

15 sites
  • Regional Clinical Hospital No1
    Ekaterinburg, Russian Federation
  • Republican Clinical Hospital of Tatarstan
    Kazan, Russian Federation
  • City Hospital n.a. V.V. Veresaev
    Moscow, Russian Federation
  • Clinical Hospital n.a. S.P. Botkin
    Moscow, Russian Federation
  • N.V. Sklifosovsky Emergency Institute
    Moscow, Russian Federation
  • National Research Center for Hematology
    Moscow, Russian Federation
  • Regional Clinical Hospital N.A. Semashko
    Nizhny Novgorod, Russian Federation
  • Regional Hospital
    Novosibirsk, Russian Federation
  • Regional Clinical Hospital
    Omsk, Russian Federation
  • RM Gorbacheva Research Institute of Pediatric Oncology, Hematology and Transplantation, Pavlov University
    Saint Petersburg, 197022, Russian Federation
  • Republican Clinical Hospital No4
    Saransk, Russian Federation
  • Republic Clinical Hospital n.a. N.A. Semashko
    Ulan-Ude, Russian Federation
  • Regional Clinical Hospital
    Vladimir, Russian Federation
  • Regional Clinical Hospital No2
    Vladivostok, Russian Federation
  • Regional Clinical Hospital
    Yaroslavl, Russian Federation
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 26, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04422470
Lead sponsor
National Research Center for Hematology, Russia
Collaborators
Foundation for Cancer Research Support (RakFond), Enrollme.ru, LLC
Responsible party
Sponsor
First posted
Jun 9, 2020
Start date
Jun 22, 2020
Primary completion
Aug 22, 2021
Completion
Jan 18, 2022
Last update
Jan 26, 2023

Study contacts

Elena Parovichnikova
study chair · National Research Center for Hematology

Oversight

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

Not currently enrolling

This study is completed, as verified in Jan 2022. You cannot join it, but the record below documents what was studied.

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