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Evaluation of the diagnostic value of copeptin combining with high-sensitivity cardiac troponin (hs-cTn) in patients with suspected non-ST-segment elevation myocardial infraction (NSTEMI)

Evaluation of the diagnostic value of copeptin combining with high-sensitivity cardiac troponin (hs-cTn) in patients with suspected non-ST-segment elevation myocardial infraction (NSTEMI)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084834
Enrollment
Unknown
Registered
2024-05-27
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-ST Elevation Myocardial Infarction (NSTEMI)

Interventions

Gold Standard:The gold standard for the diagnosis of NSTEMI follows the fourth edition of the universal definition of myocardial infarction: the detection of at least one troponin level above the 99th
(2) There is a new onset of ischemic ECG changes
(3) There is pathological Q wave on the ECG
(4) Imaging evidence, such as echocardiography or cardiac MRI, shows loss of viable myocardium or segmental wall motion abnormalities consistent with the cause of ischemia
(5) Coronary angiography or autopsy reveals thrombus formation in the coronary artery.
Index test:Copeptin
High-sensitivity Cardiac Troponin

Sponsors

Zhongshan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.The patient must be at least 18 years old. 2.The patient presented with symptoms consistent with suspected NSTEMI, including chest pain/discomfort, angina pectoris, radiating pain to the upper extremities, referred pain to the maxilla, thoracic/cervical/abdominal discomfort, dyspnea, diaphoresis, emesis/nausea, and vertigo/lightheadedness. 3.The time elapsed from symptom onset to seeking medical attention is within a 6-hour window 4.The patient agrees to comply with the relevant requirements of this research protocol.

Exclusion criteria

Exclusion criteria: 1.Patients with chest pain due to trauma 2.The patient's electrocardiogram (ECG) reveals sustained elevation of the ST segment, indicative of a ST-elevation myocardial infarction (STEMI) 3.Severe renal insufficiency requiring dialysis in end-stage renal failure patients. 4.Patients who have suffered muscle injuries or undergone major surgery within the past four weeks. 5.Pregnant and lactating individuals 6.The informed consent form is not comprehensible or agreeable to patients

Design outcomes

Primary

MeasureTime frame
Copeptin;High-sensitivity Cardiac Troponin;sensitivity;specificity;

Secondary

MeasureTime frame
Negative predictive value;Major Adverse Cardiovascular Events;

Countries

China

Contacts

Public ContactSong.zhenju

Zhongshan Hospital Affiliated to Fudan University

18301844196@sina.com+86 183 0184 4196

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026