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The Relationship Between Anesthesia Type and Inflammation After Spinal Fusion Surgery

Comparison of Remimazolam-Based and Propofol-Based Total Intravenous Anesthesia on Postoperative Inflammatory Response in One-Level Lumbar Fusion Surgery: A Prospective Randomized control Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011641
Enrollment
118
Registered
2026-02-24
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

None listed

Interventions

Drug : The intervention in this study consists of the type of hypnotic agent used for general anesthesia. Eligible participants undergoing single-level lumbar fusion surgery are randomly assigned to r

Sponsors

Yonsei University Health System, Severance Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Age: Adults aged 19 years or older (no upper age limit) Sex: Both male and female participants are eligible Diagnosis: Patients diagnosed with degenerative lumbar spine diseases (ICD-10 codes including M48.06, M48.07, M43.16, M47.26, M51.16, M54.16) Surgical procedure: Scheduled for single-level lumbar fusion surgery Anesthesia: Planned to undergo general anesthesia with total intravenous anesthesia (TIVA) Physical status: ASA physical status I–II Consent: Ability to provide written informed consent after receiving adequate explanation of the study

Exclusion criteria

Exclusion criteria: Patients receiving systemic immunosuppressive agents or systemic corticosteroids Patients with severe hepatic or renal dysfunction Patients with active infectious or inflammatory diseases Patients with a history of drug hypersensitivity reactions

Design outcomes

Primary

MeasureTime frame
Serum interleukin-6 (IL-6) concentration

Secondary

MeasureTime frame
White blood cell count (WBC);Neutrophil-to-Lymphocyte Ratio, NLR;C-reactive protein;Postoperative pain score using the Visual Analog Scale (VAS);Intraoperative opioid consumption;Total opioid consumption during the first 24 hours postoperatively (0–24 h)

Countries

Korea, Republic of

Contacts

Public ContactSooJung Park

Yonsei University Health System, Severance Hospital

crystal@yuhs.ac+82-2-2228-4430

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Mar 14, 2026