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NCT05394038 Clinical Trial

Rapid Diagnosis of Patients With Chest Pain During the Covid-19 Outbreak (My-ABCDE)

Chest Pain Clinical Trial

— My-ABCDE  

Official title:
Application of Rapid Risk Stratification for Patients Presenting With Chest Pain in the Emergency Department During the Covid-19 Outbreak in Shanghai, China.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05394038
Other study ID # My-ABCDE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2022
Est. completion date May 20, 2022

Study information
Verified date May 2022
Source Shanghai 10th People's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

During the outbreak of COVID-19, among patients with chest tightness and chest pain as the main symptoms in major medical institutions in Shanghai, China, the past medical history and rapid testing were used to quickly identify the risk stratification of the patients.

Description:

During the outbreak of COVID-19, among patients with chest tightness and chest pain as the main symptoms in major medical institutions in Shanghai, China, the past medical history and rapid testing were used to quickly identify the risk stratification of the patients. Past medical history collection includes diabetes, hypertension, coronary atherosclerotic heart disease, percutaneous coronary stent implantation, etc. Rapid detection includes rapid myocardial markers, coagulation function, electrocardiogram, chest CT, etc. Risk stratification in the shortest possible time to reduce the time patients spend congregating in hospitals and reduce unnecessary contact to reduce the risk of Covid-19 infection.

Recruitment information / eligibility
Status Completed
Enrollment 2218
Est. completion date May 20, 2022
Est. primary completion date May 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 14 Years and older
Eligibility Inclusion Criteria: - All patients who came to the hospital with chest tightness and chest pain during Covid-19. Exclusion Criteria: - None.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• None,observational study.
observational study

Locations
Country Name City State
China Shanghai Tenth People's Hospital Shanghai Shanghai

Sponsors (1)
Lead Sponsor Collaborator
Shanghai 10th People's Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Diagnosis time The time from the first medical contact to the time of diagnosis. 1 week
Secondary Diagnostic accuracy Preliminary and confirmed diagnoses were the same proportion of the total number of patients. 1week
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