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NCT04479280 Clinical Trial

Evaluation of Coagulopathy in Critically Ill COVID-19 Patients.

Coagulation Disorder Clinical Trial

Official title:
Evaluation of the Role of Sonoclot Signature in Assessment of Coagulopathy in Critically Ill COVID 19 Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04479280
Other study ID # 17300446
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 20, 2020
Est. completion date August 16, 2020

Study information
Verified date September 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Novel coronavirus disease 19 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), this pneumonia was first emerged in December 2019 in Wuhan, China and rapidly spread around the world .

Coagulopathy is one of the most significant prognostic factors in patients with COVID-19 and is associated with increased mortality and admission to critical care. Most observed coagulopathy in patients hospitalized with COVID-19 (COVID-19-associated coagulopathy) is characterized by increased D-dimer and fibrinogen levels. 71% of patients who did not survive hospitalization reported to have developed disseminated intravascular coagulation

Recruitment information / eligibility
Status Completed
Enrollment 70
Est. completion date August 16, 2020
Est. primary completion date August 16, 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- COVID 19 critically ill patients

Exclusion Criteria:

- any critical illness not related to COVID 19

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Sonclot Coagulation and platelet function Analyzer SCP1, Sienco, USA
studying coagulation disorders in COVID19 critically ill patients

Locations
Country Name City State
Egypt Assiut university Assiut

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary clot rate formation measuring how rapid the sample will get clotted 30 minutes
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