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Clinical efficacy of ultrasound-guided nerve block on analgesic management after pediatric foot orthomorphia: a randomized controlled trial

Clinical efficacy of ultrasound-guided nerve block on analgesic management after pediatric foot orthomorphia: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123434
Enrollment
Unknown
Registered
2026-04-27
Start date
2026-04-27
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Postoperative pain

Interventions

LSI group:Local surgical site infiltration
PNBs group:Peripheral nerve blocks

Sponsors

Beijing Tongren Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Foot orthopaedic surgery; 2. American Society of Anesthesiologists (ASA) Physical Status Classification I–II; 3. Body Mass Index (BMI) 16–26 kg/m^2; 4. Anaesthesia method: sevoflurane general anaesthesia; 5. Age 8-12.

Exclusion criteria

Exclusion criteria: 1. Coagulopathy, infection at the puncture site, or allergy to general or local anaesthetics; 2. Paediatric patients with a history of central nervous system disease or developmental delay; 3. Only subtalar arthroereisis implant surgery performed; 4. Anticipated surgical duration > 3 hours.

Design outcomes

Primary

MeasureTime frame
Numerical rating scale pain score, NRS;—

Secondary

MeasureTime frame
FLACC pain score;QoR-15 score;Opiod consumption;Adverse events;Sensory blosk score;Motor block score;—

Countries

China

Contacts

Public ContactChunhua Xi

Beijing Tongren Hospital, Capital Medical University

tr_xichunhua@163.com+86 136 8307 4499

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026