About this trial
This observational study aimed to investigate the prognostic value of high-frequency QRS (HF-QRS) in patients with acute myocardial infarction (AMI) after percutaneous coronary intervention (PCI), as well as its potential role in diagnosing microvascular dysfunction. The main question it aims to answer is:
1. Whether HF-QRS could serve as an effective tool for early identification of high-risk AMI patients and prognosis prediction; 2. Whether HF-QRS provides auxiliary diagnostic value for post-AMI microvascular dysfunction.
Participants underwent HF-QRS assessment and were prospectively followed for 1 year to record the incidence of major adverse cardiovascular events (MACE).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged 18 to 75 years (inclusive)
Disqualifiers
History of prior myocardial infarction or chronic heart failure
Trial population
patients with acute myocardial infarction following percutaneous coronary intervention
Trial design
Cohort
Prospective
Treatments tested in this trial
High-Frequency QRS
DeviceAll enrolled patients underwent HF-QRS assessment, with subsequent recording of MACE to evaluate the predictive value of HF-QRS parameters for clinical outcomes
Treatment groups
Trial outcomes
Primary outcomes
To evaluate the predictive value of high-frequency QRS (HF-QRS) parameters for major adverse cardiovascular events (MACE) within 1 year after PCI in AMI patients and to construct a prognostic risk prediction model.
Secondary outcomes
To evaluate the adjunctive diagnostic value of high-frequency QRS parameters for microvascular dysfunction in ACS patients following percutaneous coronary intervention
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: