NCT06488352

Brief Summary

Review the data of patients who underwent coronary artery bypass grafting (CABG) at the National Center for Cardiovascular Disease, Fuwai Hospital from January 2013 to June 2023 including medical history, head CT scan, and postoperative, including 30-day mortality, arrhythmia, cerebrovascular disease and intracerebral haemorrhage, etc. Case-control and retrospective cohort studies were conducted to explore the risk factors associated with early postoperative complications, examine their relationship with postoperative management, explore independent risk factors of compound complications, and build predictive models.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40,000

participants targeted

Target at P75+ for all trials

Timeline
1mo left

Started Jan 2013

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress99%
Jan 2013Jun 2026

Study Start

First participant enrolled

January 1, 2013

Completed
11.5 years until next milestone

First Submitted

Initial submission to the registry

June 28, 2024

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 5, 2024

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

July 5, 2024

Status Verified

June 1, 2024

Enrollment Period

13.5 years

First QC Date

June 28, 2024

Last Update Submit

June 28, 2024

Conditions

Coronary Artery Bypass

Outcome Measures

Primary Outcomes (1)

  • 30-day mortality

    The proportion of patients who die within 30 days of being admitted to the hospital.

    30 days

Secondary Outcomes (2)

  • post-operative atrial fibrillation

    Around the second postoperative day.

  • MACE

    Around the second postoperative day.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients who accepted coronary artery bypass graft and met the eligibility criteria are enrolled for this study.

You may qualify if:

  • patients accepted CABG enrolled from January 2013 to June 2023

You may not qualify if:

  • patients discharged within 72 hours of admission
  • patients with an admission diagnosis of atrial fibrillation
  • patients underwent CABG as emergency surgery
  • patients underwent concurrent surgical treatments
  • patients with repeat admissions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Structral Heart Disease Center, Fuwai Hospital

Beijing, Beijing Municipality, China

RECRUITING

Study Officials

  • Xiangbin Pan, MD

    Chinese Academy of Medical Sciences, Fuwai Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Ziping Li, MD

CONTACT

88396666ziping_li@yeah.net

Yiming Yan, MD

CONTACT

88396666yanyiming325@163.com

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

June 28, 2024

First Posted

July 5, 2024

Study Start

January 1, 2013

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

July 5, 2024

Record last verified: 2024-06

Data Sharing

IPD Sharing
Will not share

Locations

CN(1)