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Effect of preoperative continuous fascia iliaca compartment block on perioperative rapid rehabilitation quality in elderly patients with hip fracture: a randomized controlled study

Effect of preoperative continuous fascia iliaca compartment block on perioperative rapid rehabilitation quality in elderly patients with hip fracture: a randomized controlled study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040711
Enrollment
Unknown
Registered
2020-12-08
Start date
2020-11-30
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Femoral fracture

Interventions

group C:Continuous iliac fascia space block before anesthesia induction
group N:Continuous iliac fascia space block was performed after admission to the hospital

Sponsors

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 65 to 80 years old; 2. ASA grade II ~ III; 3. Diagnosis of patients with left femoral fracture undergoing primary total hip arthroplasty.

Exclusion criteria

Exclusion criteria: 1. Contraindication of nerve block: serious abnormal coagulation function, infection of the puncture site, etc.; 2. The preoperative waiting time was more than 5 days; 3. Long term use of sedatives or analgesics; the history of other psychotropic drugs; 4. Patients with severe hearing and visual impairment, unable to complete the cognitive function test, unable to complete the VAS score; 5. Morbid obesity (BMI > 35 kg / m2); 6. Allergic history of amide local anesthetics; 7. Previous history of gastrointestinal surgery, chronic gastrointestinal diseases, and chronic pain; 8. For any reason can not cooperate with the study: language understanding disorders, mental disorders, cognitive dysfunction (preoperative MMSE score < 24 points).

Design outcomes

Primary

MeasureTime frame
VAS score 2 hours after the first analgesia intervention;

Secondary

MeasureTime frame
Quality score of postoperative recovery;Antrum area;Inflammatory factor levels;

Countries

China

Contacts

Public ContactJia Mengxing

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University

Xq_1203@126.com+86 15505158136

Outcome results

None listed

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