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Propofol-opioid or Sevoflurane-opioid anaesthesia for coronary artery patients in non-cardiac surgery

Propofol-opioid or Sevoflurane-opioid anaesthesia for coronary artery patients in non-cardiac surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020502
Enrollment
Unknown
Registered
2019-01-03
Start date
2017-06-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

coronary artery patients

Interventions

Group 1:Inhaled sevoflurane
Group 2:Intravenous propofol

Sponsors

Shenzhen People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged at least 60 years old; 2. Elective or high-risk non-cardiac surgery; 3. Patients meet WHO diagnostic criteria for coronary heart disease; 4. Signing informed consent.

Exclusion criteria

Exclusion criteria: 1. Emergency surgery; 2. Low-risk surgery; 3. ASA grade V or above; 4. Combined congenital heart disease, cardiomyopathy, rheumatic heart disease, pulmonary heart disease; 5. Uncooperative (mental disorder, disturbance of consciousness, mental retardation); 6. HIV positive; 7. Secondary surgery after admission; 8. Refusal to sign informed consent.

Design outcomes

Primary

MeasureTime frame
The occurence of cardiovascular events in hospital;—

Countries

China

Contacts

Public ContactDai Zhongliang

Shenzhen People's Hospital

daizhongliang@jnu.edu.cn+86 13530756996

Outcome results

None listed

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