A Cohort of Patients Undergoing Percutaneous Coronary Intervention

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorSu Guohai

About this trial

To investigate the risk factors involved in the occurrence and prognosis of the patients with acute coronary syndrome, patients undergoing percutaneous coronary intervention will be recruited and followed up for at least 2 years.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosed as acute coronary syndrome and needed to undergo percutaneous coronary intervention.

>18 years old.

Disqualifiers

With malignant tumors, acute infectious diseases and advanced liver diseases.

Won't sign an inform consent.

Trial population

Patients with acute coronary syndrome undergoing percutaneous coronary intervention.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

major adverse cardiovascular events

all-cause mortality, cardiovascular mortality, ischemic stroke

Time frame
2-year outcome and long-term outcome

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Su Guohai

Lead sponsor

Jinan Central Hospital

Sponsor institution

Shandong First Medical University

Collaborator