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Clinical Trials/NCT04670328
NCT04670328
Completed
Not Applicable

Role of Hematological Parameters in the Stratification of COVID-19 Disease Severity

FMH College of Medicine and Dentistry1 site in 1 country101 target enrollmentMay 1, 2020
ConditionsCovid19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19
Sponsor
FMH College of Medicine and Dentistry
Enrollment
101
Locations
1
Primary Endpoint
complete blood count- Hemoglobin. White blood count, platelet count, Neutrophil to lymphocyte ratio
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The hemostatic abnormalities in COVID-19 are related with disease progression, severity and mortality. The Objective of our study is to evaluate the role of hematological parameters in determination of COVID-19 disease severity.

Detailed Description

Objective: COVID-19 virus involves respiratory as well as other body systems including cardiovascular, gastrointestinal, neurological, immunological and hematopoietic system. Patient of covid-19 pneumonia presents with wide range of hemostatic abnormalities. These hemostatic abnormalities in COVID-19 are related with disease progression, severity and mortality. The Objective of our study is to evaluate the role of hematological parameters in determination of COVID-19 disease severity. Material and Method: This was a retrospective study, conducted in Department of Pathology and Department of medicine, FMH college of Medicine and Dentistry from May 2020 to July 2020. Total of 101, confirmed cases of covid-19 disease, both genders between 17 to 75-year age were included. Hematological parameters were compared in mild, moderate, severe and critical disease group. Continuous variables were analyzed by using non parametric, Kruskal Wallis test while categorical variables were analyzed by chi-square test.

Registry
clinicaltrials.gov
Start Date
May 1, 2020
End Date
July 31, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
FMH College of Medicine and Dentistry
Responsible Party
Principal Investigator
Principal Investigator

Sadia Taj

Assistant Professor

FMH College of Medicine and Dentistry

Eligibility Criteria

Inclusion Criteria

  • diagnosed cases of covid-19 disease
  • Both genders
  • 17 to 75 year age

Exclusion Criteria

  • known case of chronic liver disease
  • known hematological diseases were excluded

Outcomes

Primary Outcomes

complete blood count- Hemoglobin. White blood count, platelet count, Neutrophil to lymphocyte ratio

Time Frame: 3 months

disease severity was assessed on basis of hematological parameters.

Secondary Outcomes

  • PT, APTT and D-dimer(3 months)

Study Sites (1)

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