perioperative atrial fibrillation incidence, risk factors and prognosis investigation in patients undergoing chest cancer surgery

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-OCS-13003282

Enrollment

Unknown

Registered

2013-06-05

Start date

2013-06-10

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Atrial fibrillation

Interventions

Case series:Nil

Eligibility

Sex/Gender

All

Age

18 Years to 110 Years

Inclusion criteria

Inclusion criteria: Patients who undergoing lung or esophageal cancer resection, ASA grade I-IV, and preoperative urine routine, liver and kidney function, blood electrolytes were in the normal range.

Exclusion criteria

Exclusion criteria: 1. Preoperative acid-base balance and electrolyte imbalance; 2. Preoperative already exists coronary heart disease, atrial fibrillation and other arrhythmias disease; 3. Patients with cardiac pacemaker; 4. Patients with severe liver and kidney dysfunction; 5. Factors such as electric knife that makes intraoperative three-channel Holter (DCG) serious disorder and unable to continue to monitor.

Design outcomes

Primary

Measure	Time frame
Atrial fibrillation;Persistent atrial fibrillation;Paroxysmal atrial fibrillation;	—

Secondary

Measure	Time frame
Hypotension<90/60mmHg;SpO2<90%;Atrial fibrillation outcome;	—

Countries

China

Contacts

Public ContactJun Fang

fangjunok@126.com+86 13606617457

Outcome results

None listed

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