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Ultrasound-Guided Combined Median Nerve and Superficial Branch of Radial Nerve Block for Analgesia in Pediatric Thumb Orthopedic Surgery

Ultrasound-Guided Combined Median Nerve and Superficial Branch of Radial Nerve Block for Analgesia in Pediatric Thumb Orthopedic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125363
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-05-26
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Congenital Thumb Deformity

Interventions

1:Ultrasound-guided combined median nerve and superficial branch of radial nerve block
2:Ultrasound-guided axillary brachial plexus block

Sponsors

Department of Anesthesiology, Children's Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 6 Years

Inclusion criteria

Inclusion criteria: Age: Children aged 1–6 years undergoing thumb surgery suitable for combined nerve block and general anesthesia. Surgery type: Planned unilateral thumb orthopedic surgery, with preoperative physician assessment indicating feasibility of either distal nerve block or brachial plexus block. ASA classification: Grade I–II (low-risk children according to the American Society of Anesthesiologists criteria). Informed consent: Written informed consent obtained from a parent or legal guardian.

Exclusion criteria

Exclusion criteria: 1. Allergy to local anesthetics or opioids; 2. Congenital or acquired neuropathy affecting sensory or motor function of the upper limb; 3. Coagulation abnormalities or current use of anticoagulant medications; 4. Infection, skin breakdown, or inflammation of the upper limb that may interfere with block performance; 5. Severe cardiac, pulmonary, hepatic, or renal dysfunction, or systemic disease (ASA >= III); 6. Previous surgery or trauma causing anatomical abnormalities of the affected upper limb that may interfere with block performance; 7. Parental refusal or inability to cooperate with follow-up assessments.

Design outcomes

Primary

MeasureTime frame
pain score;

Secondary

MeasureTime frame
Severity of upper limb motor impairment;

Countries

China

Contacts

Public ContactQing Yuan

Children's Hospital of Soochow University

85207729@qq.com+86 138 6212 0212

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026