Skip to content

Study on pain improvement of lidocaine combined with esketamine in elderly patients undergoing local anesthesia vertebroplasty

Study on pain improvement of lidocaine combined with esketamine in elderly patients undergoing local anesthesia vertebroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083466
Enrollment
Unknown
Registered
2024-04-25
Start date
2023-09-15
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Compression fracture of the lumbar spine

Interventions

LE Group:Local anesthetic use 1% lidocaine and esketamine 25mg(diluted to 20ml with normal saline)
L Group:Local anesthetic use 1% lidocaine(diluted to 20ml with normal saline)

Sponsors

Li Huili Hospital, Ningbo Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Lumbar single level percutaneous kyphoplasty; ? Age 65-80 years old; (3) American Society of Anesthesiologists (ASA) grades I-III; ? body mass index (BMI) 18.5-25 kg /m2.

Exclusion criteria

Exclusion criteria: ? Allergic to lidocaine; ? Patients who could not complete local anesthesia surgery after evaluation by the surgeon; ? Patients with severe intellectual disability who could not complete the collection of relevant indicators; ? Patients taking oral analgesics; ?Patients with esketamine allergy and mental disorders.

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
MAP, HR;MOAA/S;Adverse reaction;satisfaction;

Countries

China

Contacts

Public ContactZhou Longyuan

Li Huili Hospital, Ningbo Medical Center

396919647@qq.com+86 158 6721 2308

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026