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Randomized controlled trial for the influence of volatile anesthesia versus total intravenous anesthesia on chronic postsurgical pain after cardiac surgery using IMMPACT criteria assessment

Randomized controlled trial for the influence of volatile anesthesia versus total intravenous anesthesia on chronic postsurgical pain after cardiac surgery using IMMPACT criteria assessment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020747
Enrollment
Unknown
Registered
2019-01-16
Start date
2019-02-01
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Chronic postsurgical pain

Interventions

Group 1:volatile anesthesia
Group 2:total intravenous anesthesia

Sponsors

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

Eligibility

Sex/Gender
Male
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. aged older than 18 years; 2. received cardiopulmonary bypass for cardiac surgery via a median sternotomy; 3. signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. combined cardiac and non-cardiac surgery; 2. emergency surgery; 3. pregnancy; 4. suspected family history of malignant hyperthermia or propofol infusion syndrome; 5. failed to cooperate with follow-up because of disturbance of comprehension.

Design outcomes

Primary

MeasureTime frame
the frequency of chronic postsurgical pain ;—

Secondary

MeasureTime frame
NRS score;Opioid consumption;The Brief Pain Inventory (BPI) and McGill pain questionnaire;QoR-15;mortality;—

Countries

China

Contacts

Public ContactYu Hai

Department of Anesthesiology, West China Hospital of Sichuan University

yuhaishan117@yahoo.com+86 18980601548

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 20, 2026