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NCT04710446 Clinical Trial

Clinical Characteristics, Treatments, and Outcomes of MI Patients Presenting With Normal ECG

Electrocardiography Clinical Trial

Official title:
Clinical Characteristics, Treatments, and Outcomes of MI Patients Presenting With Normal ECG

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04710446
Other study ID # Normal MI
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2018
Est. completion date January 2023

Study information
Verified date August 2022
Source Henan Provincial People's Hospital
Contact qiongya Guo
Phone 18838067197
Email gqy19870203@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

the investigators aimed to analyzed data for hospitalized MI patients with normal ECG.

Description:

The electrocardiogram (ECG) at presentation is a useful tool for risk prediction. Patients with ACS（Acute Coronary Syndromes） and ST-segment depression on ECG have a worse prognosis than patients with a normal ECG. ST-segment depression is not only a qualitative marker, but also a quantitative marker of risk, because the number of leads with ST-segment depression and the magnitude of ST-segment depression (either within a single lead or as sum over all leads) are indicative of the extent of ischaemia and correlate with prognosis.The presence of ST-segment depression >1 mm in >_6 leads in conjunction with ST-segment elevation in aVR and/or V1, particularly if the patient presents with haemodynamic compromise, suggests multivessel ischaemia or severe left main coronary artery stenosis. However,in patients presenting without persistent ST-segment elevation,the clinical features, treatments, and outcomes in patients with normal ECG is still unclear.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date January 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 100 Years
Eligibility Inclusion Criteria:all patients hospitalized with a principal diagnosis of non-ST-segment elevation infarction (NSTEMI) according to the current ACC/AHA guidelines. exclusion criteria: end-stage organic disease, thrombotic hematological disorders, and poor echogenicity

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
China Henan province people's hospital Zhengzhou Henan

Sponsors (1)
Lead Sponsor Collaborator
Henan Provincial People's Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary MACE within 2 weeks Major Adverse Cardiovascular Events within2 weeks within 2 weeks
Primary MACE within 1 year Major Adverse Cardiovascular Events in-hospital within 1 year within 1 year
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