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Prospective Multicenter Study for Early Evaluation of Acute Chest Pain

NCT04122573 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2019-11-29

No results posted yet for this study

Summary

In this study, clinical database and blood sample bank of acute chest pain (ACP) will be established at chest pain center of multi-center hospital. To explore new biomarkers and screen clinical indicators with effective risk stratification and prognostic evaluation for ACP through proteomics technology and statistics methods. Risk stratification and short-term and long-term prognostic evaluation models for high-risk ACP will be established using large data analysis.

Conditions

Interventions

DIAGNOSTIC_TEST

Coronary angiography

Acute chest pain patients, suspected acute coronary syndrome, are diagnosed by coronary angiography.

DIAGNOSTIC_TEST

CT angiography of aorta

Acute chest pain patients, suspected acute aortic dissection, are diagnosed by gold standard of CTA.

DIAGNOSTIC_TEST

CT angiography of pulmonary arteries.

Acute chest pain patients, suspected acute pulmonary embolism, are diagnosed by gold standard of CTA.

DIAGNOSTIC_TEST

Electrocardiogram

All patients with acute chest pain will subject to ECG examination within 10 minutes of admission, which can quickly screen ST-segment elevation myocardial infarction.

DIAGNOSTIC_TEST

Cardiac Troponin

Dynamic changes of cardiac troponin I and/or T will be used in the diagnosis of acute myocardial infarction

Sponsors & Collaborators

  • West China Hospital

    lead OTHER

Principal Investigators

  • Dongze Li, MBBS · Emergency Department, West China Hospital, Sichuan University

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-11-01
Primary Completion
2021-10-31
Completion
2022-10-31

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04122573 on ClinicalTrials.gov