Pulmonary Embolism and COVID-19
COVID-19-PE
Evaluation of the Patients With COVID-19 in Terms of Pulmonary Embolism
1 other identifier
observational
600
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2020
CompletedFirst Submitted
Initial submission to the registry
October 14, 2020
CompletedFirst Posted
Study publicly available on registry
October 19, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2021
CompletedMay 4, 2021
May 1, 2021
1.3 years
October 14, 2020
May 1, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
pulmonary embolism
development of pulmonary embolism
1 year
Secondary Outcomes (2)
Intensive care unit
1 year
mortality
1 year
Study Arms (2)
Covid-19 Patients with Pulmonary embolism
Clinically demonstared cases infected with COVID-19 who developed pulmonary embolism.
Covid-19 Patients without Pulmonary embolism
Clinically demonstared cases infected with COVID-19 who did not develop pulmonary embolism.
Interventions
intensive care unit admission ratio
Eligibility Criteria
All COVID-19 patients with positive RT-PCR tests will be analyzed retrospectively. Patients with and without pulmonary embolism will be compared in terms of age, gender, side disease, hospitalization in intensive care, mortality rates etc.
You may qualify if:
- \- All patients with positive RT-PCR for COVID-19
You may not qualify if:
- \- All patients with negative RT-PCR for COVID-19
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Uşak Universitylead
Study Sites (1)
Uşak University
Uşak, 64200, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Cevdet Duran, M.D.
Uşak University Medical School
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 14, 2020
First Posted
October 19, 2020
Study Start
March 1, 2020
Primary Completion
June 1, 2021
Study Completion
December 1, 2021
Last Updated
May 4, 2021
Record last verified: 2021-05
Data Sharing
- IPD Sharing
- Will not share