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Application of ultrasound-guided iliac fascial space block based on deep circumflex iliac artery positioning in perioperative analgesia in elderly patients with hip fracture

Application of ultrasound-guided iliac fascial space block under deep circumflex iliac artery positioning in perioperative analgesia in elderly patients with hip fracture

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044772
Enrollment
Unknown
Registered
2021-03-27
Start date
2021-03-31
Completion date
Unknown
Last updated
2021-10-26

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

Conditions

Hip fracture

Interventions

control group:Inguinal ligament level iliac fascial space block
experimental group:Iliac fascial space block group under location of deep circumflex iliac Artery

Sponsors

Department of Anesthesiology, Subei People's Hospital of Jiangsu province
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 65 to 85 years; 2. ASA classification is I and II; 3. Hip surgery; 4. The subjects (or their legal representatives) have signed the informed consent form.

Exclusion criteria

Exclusion criteria: The following patients cannot participate in this study: 1. There is a history of myocardial infarction or unstable angina pectoris, or atrioventricular block of degree II and above within 6 months, or a history of severe arrhythmia such as stagnation, or a history of NYHA heart function class II and above before screening ; 2. Past mental system diseases (such as schizophrenia, depression, etc.) and cognitive dysfunction, or a history of epilepsy,or a history of Parkinson's syndrome; 3. Subjects who have not received regular antihypertensive therapy or have poor blood pressure control (systolic blood pressure >= 160mmHg or = 100mmHg or = 11.1mmol/L; 5. Abnormal coagulation function during the screening period: prothrombin time (PT) prolonged beyond the upper limit of normal by 3 seconds and/or activated partial thromboplastin time (APTT) prolonged beyond the upper limit of normal by 10 seconds; 6. Consecutive taking opioid analgesics for more than 10 days, or the time of last taking the drug is less than the 5 half-life of the drug at random.

Design outcomes

Primary

MeasureTime frame
a numerical rating scale (NRS) score;Sensory block duration;Morphine consumption;Serum C-reactive protein (CRP) and interleukin-6 (IL-6);

Countries

China

Contacts

Public ContactWang Cunjin

Department of Anesthesiology, Subei People's Hospital of Jiangsu province

zebra1987@126.com+86 18051061453

Outcome results

None listed

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