Effect of Xuesaitong Soft Capsules on Major Risk Factors in Patients With Coronary Heart Disease

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorChina National Center for Cardiovascular Diseases

About this trial

This trials aims to assess, in 240 eligible patients with coronary heart disease, the effects on level of high-sensitivity C-reactive protein (hsCRP) changes from baseline to 12 weeks of Xuesaitong Soft Capsules.

Eligibility criteria

Qualifiers

Age ≥18 years old

History of myocardial infarction

Have received coronary interventional therapy

There are symptoms of myocardial ischemia (such as chest pain) and objective evidence (stress electrocardiogram or stress myocardial perfusion imaging indicated myocardial ischemia or coronary artery stenosis ≥50% )

Disqualifiers

Acute coronary syndrome occurred or received percutaneous coronary intervention therapy within the past 3 months

Previously received coronary artery bypass grafting

Stroke occurred within the previous 3 months

Symptomatic heart failure (HF) in the past, or documented left ventricular ejection fraction < 35%

Trial design

Treatments tested in this trial

  • Xuesaitong Soft Capsule
  • Placebo

Treatment groups

240 Participants
are divided into 2 treatment groups