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Clinical Trials/NCT04422470
NCT04422470
Completed
N/A

Observational Prospective Cohort Study - Registry of Patients With Hematologic Disease and COVID-19 in Russia (CHRONOS19)

National Research Center for Hematology, Russia13 sites in 1 country666 target enrollmentJune 22, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Coronavirus Infection and Hematologic Diseases
Sponsor
National Research Center for Hematology, Russia
Enrollment
666
Locations
13
Primary Endpoint
30-day all-cause mortality
Status
Completed
Last Updated
3 years ago

Overview

Brief 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).

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.

Registry
clinicaltrials.gov
Start Date
June 22, 2020
End Date
January 18, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

30-day all-cause mortality

Time Frame: 30 day

Rate of death from any cause

Secondary Outcomes

  • Relapse or progression of hematologic disease(30 day, 90 day and 180 day)
  • Overall survival(30 day, 90 day and 180 day)
  • ICU admission(30 day)
  • COVID-19 complications(30 day)
  • Mechanical ventilation / O2 requirement(30 day)
  • Risk factors(30 day, 90 day and 180 day)

Study Sites (13)

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