Study on the Effect of Target-controlled Infusion for General Anesthesia in Cardiac Surgery

Recruiting

• Conditions: Postoperative Mechanical Ventilation Time

• Registration Number: NCT06012955
• Lead Sponsor: Wuhan Union Hospital, China

Brief Summary

The purpose of the study was to evaluate whether individualized general anesthesia with target-controlled infusion could help patients wake up early for extubation and reduce the incidence of postoperative complications, and to investigate the effectiveness and safety of its application in patients undergoing cardiac surgery.

Detailed Description

Not available

Study Timeline

• Status Verified: 2023-08
• Study First Submitted: 2023-08-20
• Study First Submitted QC: 2023-08-25
• Last Update Submitted: 2023-08-25
• Study First Posted: 2023-08-28
• Last Update Posted: 2023-08-28
• Study Start: 2023-08-30
• Primary Completion: 2023-12-31
• Study Completion: 2024-06-30

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 2000

Inclusion Criteria

• All patients aged 18 years and older who underwent cardiac surgery

Exclusion Criteria

• Mechanical ventilation support before surgery;
• Combined with any type of non-cardiac surgeries;
• Second exploratory thoracotomy after surgery;
• Died or discharged within 48 h after surgery;
• Missing clinical data

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of postoperative mechanical ventilation	4 weeks after surgery	Duration of mechanical ventilation was defined as the time from the end of surgery to tracheal extubation

Trial Locations

Locations (1)

Wuhan Union Hospital; 🇨🇳 Wuhan, Hubei, China