Assessment of the Diagnostic Performance of the Detection System and Establishment of an Intelligent and Rapid Triage Model

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChina National Center for Cardiovascular Diseases

About this trial

The rapid triage of patients with acute chest pain remains an important issue in clinical practice. This study will establish a cohort of patients suspected of acute coronary syndrome (ACS) to construct a multi-marker dynamic combined intelligent triage model. This model will triage the risk of NSTEMI in patients with chest pain at their first visit. It will also stratify the risk of patients with chest pain using major adverse cardiovascular events (MACE) within 30 days as the endpoint.

Eligibility criteria

Qualifiers

Adults aged 18 years or above from China, regardless of gender;

Presence of symptoms such as chest tightness and chest pain, with the need to determine whether they are patients with acute coronary syndrome;

Ability to obtain informed consent.

Disqualifiers

- Patients with STEMI at the time of presentation;

Patients with a clear diagnosis after tests such as troponin;

Patients who have undergone major surgery or trauma within the past four weeks;

Pregnant women or patients with tumors undergoing radiotherapy or chemotherapy;

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Locations

This trial has no locations

Sponsors and collaborators

China National Center for Cardiovascular Diseases

Lead sponsor

Chinese Academy of Medical Sciences, Fuwai Hospital

Collaborator