None
Conditions
Interventions
Experimental group:Perform nerve block on the experimental group patients
Control group:The control group patients were given oral analgesics as needed
Sponsors
Kaifeng Central Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: (1) Admitted within 12 hours after trauma, diagnosed with traumatic fracture through X-ray examination and meeting relevant orthopedic diagnostic criteria; (2) American Anesthesiologist Classification (ASA) II-III; (3) Meets the indications for orthopedic surgery; (4) Age >= 18 years old; (5) Informed consent for this study.
Exclusion criteria
Exclusion criteria: (1) Combined dysfunction of important organs such as heart, liver, kidney, and nervous system; (2) Combined immunodeficiency or immune related diseases; (3) Patients with poor treatment compliance; (4) Contraindications related to nerve block, such as coagulation dysfunction and local or systemic infections.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cortisol;C-reactive protein;ß - endorphin;IL-10; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual analog pain score at rest;Visual simulation pain rating during activities; | — |
Countries
China
Contacts
Public ContactGuozhong Yan
Kaifeng Central Hospital
Outcome results
None listed