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RecruitingNCT06488352OptiCABGUpdated Jul 5, 2024

Enhancing Care Study in Patients After CABG

An observational study in Coronary Artery Bypass, sponsored by Chinese Academy of Medical Sciences, Fuwai Hospital. Recruiting at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-07-05.

Sponsored by Chinese Academy of Medical Sciences, Fuwai Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Jun 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Jan 2013; still recruiting 13 years 9 months later.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
40,000
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Coronary Artery Bypass
03

In context

Lead sponsor

Chinese Academy of Medical Sciences, Fuwai Hospital is the lead sponsor of 141 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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

Inclusion criteria

  • patients accepted CABG enrolled from January 2013 to June 2023

Exclusion criteria

Exclusion Criteria:

  • 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
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
40,000 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. 30-day mortality

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

    Time frame: 30 days

Secondary outcomes

  1. post-operative atrial fibrillation

    The occurrence of atrial fibrillation after a patient has undergone surgery.

    Time frame: Around the second postoperative day.

  2. MACE

    A combination of several critical cardiovascular events may vary depending on the specific context of the study or clinical evaluation.

    Time frame: Around the second postoperative day.

07

Study locations

1 of 1 sites recruiting
  • Structral Heart Disease Center, Fuwai Hospital
    Beijing, Beijing, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06488352
Lead sponsor
Chinese Academy of Medical Sciences, Fuwai Hospital
Responsible party
Pan Xiangbin (Principal Investigator, Chinese Academy of Medical Sciences, Fuwai Hospital) — Principal investigator
First posted
Jul 5, 2024
Start date
Jan 1, 2013
Primary completion
Jun 30, 2026 (estimated)
Completion
Jun 30, 2026 (estimated)
Last update
Jul 5, 2024

Study contacts

Ziping Li, MD
Contact
ziping_li@yeah.net
88396666
Yiming Yan, MD
Contact
yanyiming325@163.com
88396666
Xiangbin Pan, MD
principal investigator · Fuwai Hospital, CAMS & PUMC

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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