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Ultrasound-guided nerve block for preemptive analgesia in elderly patients with hip fracture : a single-center prospective randomized controlled study

Ultrasound-guided nerve block for preemptive analgesia in elderly patients with hip fracture : a single-center prospective randomized controlled study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102361
Enrollment
Unknown
Registered
2025-05-13
Start date
2025-05-31
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

hip joint fracture

Interventions

Test group :Using 133 mg bupivacaine liposomes ( Jiangsu Hengrui Medicine
266mg ) 20ml for hip joint capsule peripheral nerve block
Control group:According to the needs of patients, non-steroidal analgesics were given for analgesic treatment.

Sponsors

Henan Provincial People's Hospita,medical
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with unilateral hip fracture at admission, 65 years old <= age <= 80 years old, ASA grade I-III, normal sensory and motor function before injury. 2. Before the test, the nature, significance, possible benefits, possible inconveniences, potential risks and discomforts of the test were fully understood, and the informed consent was voluntarily participated in and signed. 3. The patient is conscious and has normal cognitive ability, and can complete the questionnaire independently or with the help of the researcher. 4. No corresponding nerve block operation area infection; 5. Patients with visual analogue scale ( VAS score ) = 4 at the time of orthopedic treatment.

Exclusion criteria

Exclusion criteria: 1. Don 't understand or reject research methods. 2. Allergic to any of the drug components in the study; 3. There are contraindications for nerve block or the use of drugs in this study. 4. There are cognitive dysfunction, Alzheimer 's disease or mental illness; 5. Two or more fractures; 6. Severe liver and kidney dysfunction; 7. Severe coagulation dysfunction; 8. Long-term history of taking analgesic drugs; 9. gastrointestinal bleeding; 10. Intervention less than 48 hours from surgery;

Design outcomes

Primary

MeasureTime frame
Different time periods of exercise ( different time periods of exercise ( passive hip flexion leg lift 15 ° ) VAS pain score.;

Secondary

MeasureTime frame
Static VAS pain scores at different time periods;rate of complications;Hemodynamic indexes at different time periods;quality of sleep of patients;Total consumption of analgesics;incidence of postoperative delirium;patient satisfaction;

Countries

China

Contacts

Public ContactMingzhu Cui

Henan Provincial People's Hospita,medical

cuimingzhu78@163.com+86 186 3900 6993

Outcome results

None listed

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