Construction of a Prospective Cohort Database for the Perioperative Period of Cardiac Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

Cardiovascular disease (CVD) is the leading cause of global morbidity and mortality, with its prevalence increasing significantly from 1990 to 2019. Establishing a comprehensive cardiac surgery database is crucial for exploring perioperative prognostic factors and improving clinical outcomes.

This muti-center, prospective observational study aims to construct a prospective cohort database for perioperative cardiac surgery. We plan to enroll adult patients who undergo cardiac surgery with cardiopulmonary bypass at the Second Affiliated Hospital of Zhejiang University and other hospitals from May 1, 2026 to December 31, 2031. Multi-dimensional perioperative data, including laboratory tests, hemodynamics, intraoperative echocardiography, and perioperative medications, will be collected and integrated, along with epidemiological data, clinical diagnosis and treatment information, multimodal data, and follow-up outcomes. An interconnected big data sharing platform will also be built.

This database will provide a valuable resource for multi-level researches such as perioperative risk assessment, individualized prevention, precise diagnosis and treatment, and therapeutic efficacy monitoring. It will also help optimize surgical and perioperative management, improve the quality of cardiac surgery, and provide evidence for the refinement of China's healthcare system, ultimately enhancing perioperative safety and rehabilitation efficiency of patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients undergoing cardiac surgery from May 1, 2026 to December 31, 2031

Disqualifiers

Refusal to provide informed consent

Trial population

Patients undergoing cardiac surgery from May 1, 2026 to December 31, 2031

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Cardiac surgey

    Procedure/Surgery

    Cardiac surgey

Treatment groups

10,000 Participants
are divided into 1 treatment group
Group A: Perioperative Observation Group1 intervention

Trial outcomes

Primary outcomes

1

Incidence of major adverse cardiac and cerebrovascular events (MACCE)

Myocardial infarction; New-onset stroke: new irreversible neurological impairment confirmed by radiological examination or autopsy showing a new cerebral lesion; Death

Time frame
4, 12 weeks and 1years after surgery
2

Incidence of Perioperative Transfusion of Allogeneic Blood Products

Allogeneic red blood cells, plasma, platelets, and blood coagulation factors

Time frame
30 days after surgery
3

Amount of Allogeneic Blood Products Transfused During the Perioperative Period

Allogeneic red blood cells, plasma, platelets, and blood coagulation factors

Time frame
30 days after surgery

Secondary outcomes

1

Incidence of perioperative myocardial infarction

Myocardial infarction

Time frame
4, 12 weeks and 1years after surgery
2

Incidence of New-onset stroke

New-onset stroke: new irreversible neurological impairment confirmed by radiological examination or autopsy showing a new cerebral lesion

Time frame
4, 12 weeks and 1years after surgery
3

Incidence of death

death

Time frame
4, 12 weeks and 1years after surgery
4

Incidence of acute kidney injury

acute kidney injury was defined by guidelines of kindey disease:improving global outcomes(KIDGO)

Time frame
7days after suegery

Other outcomes

Sponsors and contacts

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