- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04670328
Role of Hematological Parameters in the Stratification of COVID-19 Disease Severity
Studieoversigt
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- FMH college of medicine and dentistry
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Covid-19 disease severity
Mild, moderate, severe and critical disease
|
Diagnostic tests( hematological parameters) were assessed.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
complete blood count- Hemoglobin. White blood count, platelet count, Neutrophil to lymphocyte ratio
Tidsramme: 3 months
|
disease severity was assessed on basis of hematological parameters.
|
3 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
PT, APTT and D-dimer
Tidsramme: 3 months
|
improvement in PT, APTT and D-dimer levels were assessed
|
3 months
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
LDH, serum ferritin level
Tidsramme: 3 months
|
improvement in LDH and were assessed
|
3 months
|
Samarbejdspartnere og efterforskere
Efterforskere
- Studiestol: Ayaz Lone, MBBS,FCPS, FMH college of medicine and dentistry
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- FMHCMD
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
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