Clinical study on early warning of perioperative myocardial injury in patients with non-cardiac major surgery by TEG

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900028592

Enrollment

Unknown

Registered

2019-12-28

Start date

2020-01-01

Completion date

Unknown

Last updated

2020-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perioperative myocardial injury

Interventions

Gold Standard:Clinical outcome

Index test:thrombelastogarm

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: High risk patients with perioperative myocardial damage.

Exclusion criteria

Exclusion criteria: 1. patients with mental disorders;cardiac surgery; 2. patients who refused to participate in this study or to follow up.

Design outcomes

Primary

Measure	Time frame
Troponin was observed and recorded one day after surgery;SEN, SPE, ACC, AUC of ROC;	—

Secondary

Measure	Time frame
The incidence and mortality of MACE at 1 and 3 months after surgery;	—

Countries

China

Contacts

Public ContactZeping Dai

The First Affiliated Hospital of Wannan Medical College

hwldzp@163.com+86 13955365823

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026