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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04590378
Other study ID # UU-PE001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2020
Est. completion date December 1, 2021

Study information

Verified date May 2021
Source Usak University
Contact Cevdet Duran, M.D.
Phone +905334298585
Email drcduran@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The charts of patients who developed pulmonary embolism in the course of COVID-19 will be evaluated, retrospectively. Clinical features and laboratory data will be analyzed.


Description:

Patients with COVID-19 infection will be evaluated retrospectively. Demographic data, clinical and laboratory findings will be recorded. Findings of patients with pulmonary embolism and withour pulmonary embolism will be compared.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date December 1, 2021
Est. primary completion date June 1, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - All patients with positive RT-PCR for COVID-19 Exclusion Criteria: - All patients with negative RT-PCR for COVID-19

Study Design


Related Conditions & MeSH terms


Intervention

Other:
intensive care unit admission ratio
intensive care unit admission ratio

Locations

Country Name City State
Turkey Usak University Usak

Sponsors (1)

Lead Sponsor Collaborator
Usak University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary pulmonary embolism development of pulmonary embolism 1 year
Secondary Intensive care unit need for admission to intensive care unit 1 year
Secondary mortality mortality rate due to pulmonary embolism 1 year
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