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Ultrasound-guided suprainguinal fascia iliaca compartment block versus caudal block for postoperative analgesia in pediatric undergoing hip reconstruction surgery:a prospective randomized controlled trial

Ultrasound-guided suprainguinal fascia iliaca compartment block versus caudal block for postoperative analgesia in pediatric undergoing hip reconstruction surgery:a prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105607
Enrollment
Unknown
Registered
2025-07-07
Start date
2025-07-07
Completion date
Unknown
Last updated
2025-07-14

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

Conditions

None

Interventions

Fascia iliaca block group:ultrasound-guided fascia iliaca block
Caudal block group:Caudal block

Sponsors

Children’s Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1.Age between 1 and 18 years 2.Scheduled for elective hip reconstruction surgery 3.ASA physical status I-II

Exclusion criteria

Exclusion criteria: 1. Agree to participate in the study; 2. Return to the intensive care unit after surgery; 3. Contraindications to regional block (such as allergy to local anesthetics, infection at the puncture site of the block, abnormal coagulation function, anatomical deformity, rejection of regional block, etc.); 4. BMI > 95% of children of the same age; 5. Bilateral surgery; 6. History of previous regional block puncture site surgery; 7. History of chronic pain; 8. Patients with mental retardation;

Design outcomes

Primary

MeasureTime frame
Cumulative opioid consumption the first 24 h after hip reconstruction surgery;

Secondary

MeasureTime frame
Postoperative 24-hour pain scores;Occurrence of adverse events;

Countries

China

Contacts

Public ContactYun Shi

Children’s Hospital of Fudan University

shi_yun@fudan.edu.cn+86 139 1826 8351

Outcome results

None listed

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