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The Effect of Lidocaine on Cognitive Function in Patients after Unilateral Biportal Endoscopic Spine Surgery

The Effect of Lidocaine on Cognitive Function in Patients after Unilateral Biportal Endoscopic Spine Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117219
Enrollment
Unknown
Registered
2026-01-21
Start date
2026-01-21
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Cognitive Impairment

Interventions

Experimental Group:Administer a loading dose of 1.0 mg/kg lidocaine first, then maintain continuous intravenous infusion of 1.0 mg/kg lidocaine till surgery completion.
Control group:Administer equal doses of normal saline infusion

Sponsors

Shihezi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Elderly patients (of either gender) scheduled for elective UBE surgery; 2. Age range: 60 - 85 years old; 3. BMI: 18 - 28 kg/m^2; 4. ASA I-II grade; 5. Education level: primary school or above; 6. No obvious heart or lung diseases, normal communication skills; 7. Voluntary and willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe heart, liver or kidney diseases; 2. Long-term use of opioid drugs; 3. Allergy or contraindication to lidocaine; 4. Anxiety and/or depression; 5. Surgical death, massive bleeding during surgery, requiring blood transfusion, and needing to be transferred to the intensive care unit for further treatment after surgery; 6. Those with unclear ultrasound temporal window imaging.

Design outcomes

Primary

MeasureTime frame
Cognitive level assessment results;

Secondary

MeasureTime frame
Hemodynamic indicators;Surgical-related indicators;

Countries

China

Contacts

Public ContactXiuling Wu

Shihezi People's Hospital

dengwen0703@126.com+86 993 205 1039

Outcome results

None listed

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