Hip Fracture
Conditions
Interventions
Bupivacaine group :Bupivacaine liposome infiltration anesthesia
Control group:Without bupivacaine liposome infiltration anesthesia
Sponsors
Beijing Jishuitan Hospital, Capital Medical University
Eligibility
Sex/Gender
All
Age
65 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Trauma orthopedics plans to perform hip fracture surgery; 2. ASA grade I~ III; 3. Not less than 65 years old, gender not limited; 4. Capable of language expression or reading, able to independently or with the help of a physician understand and complete survey questionnaires, and agree to participate in the study.
Exclusion criteria
Exclusion criteria: 1. Patients with combined mental system disorders and cognitive dysfunction; 2. Combined sensory disorders such as hyperalgesia or other physical pain that affects postoperative pain assessment; 3. Allergy to bupivacaine or other amide local anesthetics, as well as severe liver or renal dysfunction; 4. Patients with any other factors that are not suitable for participating in this trial. There are mental illnesses, consciousness disorders, and communication barriers present.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS score ; | — |
Secondary
| Measure | Time frame |
|---|---|
| Time from operation to discharge (hour);Complication ; Sleep quality assessment ;Dosage of Tramadol ;Postoperative ambulation time ;Patient pain satisfaction score at 72 hours after surgery ;Number of compressions of analgesic pump ;The total consumption of opioid drugs from the end of surgery to 72 hours after surgery;The incidence of delirium within 3 days after surgery; | — |
Countries
China
Contacts
Public ContactLi Ting
Beijing Jishuitan Hospital, Capital Medical University
Outcome results
None listed