Status:

UNKNOWN

Suxiao Jiuxin Pills in Microvascular Obstruction in Patients With Acute Coronary Syndrome

Lead Sponsor:

Guangzhou University of Traditional Chinese Medicine

Conditions:

Acute Coronary Syndrome

Eligibility:

All Genders

18-75 years

Phase:

PHASE4

Brief Summary

Microvascular obstruction is the severe complication of percutaneous coronary intervention (PCI) in patients with acute coronary syndrome. Microvascular obstruction after PCI is often association with...

Eligibility Criteria

Inclusion

  • Meet the diagnosis of AMI, prepare for PCI reperfusion therapy;
  • Between the ages of 18-75;
  • Volunteer to participate in this study and have signed an informed consent form;
  • Have a correct understanding of the significance of drug research, and have a good compliance with the observation and evaluation.

Exclusion

  • Not suitable for coronary intervention;
  • With unstable hemodynamics;
  • Platelet count\<100×109;
  • Suspected aortic dissection or acute pulmonary embolism;
  • With mechanical complications;
  • With uncontrolled acute left heart failure and pulmonary edema;
  • With known bleeding history, active bleeding, bleeding constitution, or severe hemostatic and coagulation dysfunction;
  • Meantain anticoagulants (such as warfarin or new anticoagulants);
  • Severe liver and kidney insufficiency (Child-Pugh B and above, Cr\>177μmol/L (2mg/dl) or eGFR\<45ml/min/1.73m2);
  • CTO, stent stenosis, or severe left main disease;
  • History of coronary artery bypass graft surgery;
  • Other pathophysiological conditions whose expected survival period is less than 1 year;
  • Allergic history to Suxiao Jiuxin Pills;
  • Pregnant or lactating women;
  • Participating in other clinical studies;
  • With other diseases that are not suitable for participating in clinical research.

Key Trial Info

Start Date :

May 1 2021

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

September 30 2023

Estimated Enrollment :

198 Patients enrolled

Trial Details

Trial ID

NCT04814121

Start Date

May 1 2021

End Date

September 30 2023

Last Update

March 24 2021

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