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Clinical outcomes of volatile anesthesia versus total intravenous anesthesia for patients undergoing heart valve surgery: a randomized controlled trial

Clinical outcomes of volatile anesthesia versus total intravenous anesthesia for patients undergoing heart valve surgery: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021298
Enrollment
Unknown
Registered
2019-02-12
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-02-18

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

Conditions

heart valve disease

Interventions

volatile group:volatile anesthesia
TIVA group:total intravenous anesthesiaotal intravenous anesthesia, TIVA

Sponsors

Department of Anesthesiology, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. aged older than 18 years; 2. undergoing heart valve surgery under CPB; 3. signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Non-valve surgery such as CABG, aorta; 2. valve surgery combined with CABG; 3. combined cardiac and non-cardiac surgery; 4. emergency surgery; 5. Pregnancy; 6. suspected family history of malignant hyperthermia or propofol infusion syndrome; 7. failed to cooperate with follow-up because of disturbance of comprehension.

Design outcomes

Primary

MeasureTime frame
a composite of major complications during hospitalization and death from any cause occurring within the first 30 days after surgery;

Secondary

MeasureTime frame
mortality;postoperative mechanical ventilation time;length of stay in ICU;length of stay in hospital;

Countries

China

Contacts

Public ContactYu Hai

Department of Anesthesiology, West China Hospital, Sichuan University

yuhaishan117@yahoo.com+86 18980601548

Outcome results

None listed

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