Role of low-dose of propofol in prediction of perioperative risk in cardiac surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100046087

Enrollment

Unknown

Registered

2021-05-04

Start date

2021-05-10

Completion date

Unknown

Last updated

2021-12-13

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

Conditions

anesthesia risk

Interventions

Case series:low-dose propofol

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Cardiac surgery with cardiopulmonary bypass 2. Older than 18 years; 3. Operation duration is longer than 1 hour; 4. Informed consent has been signed.

Exclusion criteria

Exclusion criteria: 1. Allergic to fat emulsion; 2. Preoperative disturbance of consciousness; 3. Predicted difficult airway;

Design outcomes

Primary

Measure	Time frame
Blood pressure;	—

Countries

China

Contacts

Public ContactWei Wei

West China Hospital, Sichuan University

111weiwei@sohu.com+86 18980601544

Outcome results

None listed

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