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Comparison of pain outcomes after radical gastrectomy between propofol and sevoflurane anesthesia

Comparison of pain outcomes after radical gastrectomy between propofol and sevoflurane anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15006472
Enrollment
Unknown
Registered
2015-05-31
Start date
2015-06-29
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

perioperative pain management

Interventions

Propofol group:Propofol
Sevoflurane group:Sevoflurane

Sponsors

Department of Anesthesiology, the First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients between the ages of 18 and 65 years with ASA classification17 of I or II undergoing radical gastrectomy were eligible for inclusion in the study

Exclusion criteria

Exclusion criteria: Exclusion criteria were known allergy to medications used in this study, obesity, ASA classification III or more, severe cardiac or respiratory problems, severe hepatic or renal diseases, uncooperative

Design outcomes

Primary

MeasureTime frame
pain scores;sedation scores;PONV;satisfaction scores;—

Countries

China

Contacts

Public ContactFu-hai Ji
jifuhai@hotmail.com+86 13656207331

Outcome results

None listed

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