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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04399681
Other study ID # KSSEAH--
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 10, 2020
Est. completion date September 10, 2020

Study information

Verified date May 2020
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact Ramazan Guven
Phone +902124041500
Email drramazanguven@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Novel Coronavirus 2019 Disease (COVID-19) mortality is highly associated with viral pneumonia and its complications. Accurate and prompt diagnosis shown to be effective to improve outcome by providing early treatment strategies. While chest X-ray (CXR) and computerized tomography (CT) are defined as gold standard, given the advantage of being an ionized radiation free, practical technique point of care ultrasound (POCUS) is also reported as a diagnostic tool for COVID-19. There are limited studies regarding the importance of POCUS in diagnosis and review of COVID-19. Therefore the aim of this study is to evaluate the utility of bedside lung ultrasound on diagnosis of COVID-19 for patients admitted to emergency department .


Description:

Novel Coronavirus 2019 Disease (COVID-19) mortality is highly associated with viral pneumonia and its complications. Accurate and prompt diagnosis shown to be effective to improve outcome by providing early treatment strategies. While chest X-ray (CXR) and computerized tomography (CT) are defined as gold standard, given the advantage of being an ionized radiation free, practical technique point of care ultrasound (POCUS) is also reported as a diagnostic tool for COVID-19. There are limited studies regarding the importance of POCUS in diagnosis and review of COVID-19. Therefore the aim of this study is to evaluate the utility of bedside lung ultrasound on diagnosis of COVID-19 for patients admitted to emergency department .


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 10, 2020
Est. primary completion date August 10, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All patients with an informed consent

- Admission to emergency department with symptoms or signs of COVID-19

Exclusion Criteria:

- Absence of informed consent

- Patients under age of 18

- Presence of acute coronary syndrome

- Presence of chronic lung disease

- Pregnancy

- Presence of trauma

- Patients with a diagnosis of malignancy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Bedside lung ultrasound
Point of care ultrasound will be used as bedside lung ultrasound to determine the patients if they have a COVID-19 pneumonia.

Locations

Country Name City State
Turkey Istanbul Kanuni Sultan Suleyman Training and Research Hospital Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Presence of viral pneumonia caused by COVID 19 Efficacy of POCUS on diagnosis of viral pneumonia caused by COVID 19 3 months
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