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Clinical Research of the Multimodal Ultrasound in Brachial Plexus Injury.

Clinical Research of the Multimodal Ultrasound in Brachial Plexus Injury.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112807
Enrollment
Unknown
Registered
2025-11-19
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Brachial Plexus Injury

Interventions

Gold Standard:the MRI exam finding of brachial plexus

Sponsors

Jing'an District Central Hospital of Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients to be diagnosed with suspected severe brachial plexus nerve injury resulting in limb dysfunction. 2. Patients with suspected brachial plexus injury proposed to be diagnosed with nerve root avulsion or rupture. 3. Patients with suspected brachial plexus injury who have a clear history of upper limb brachial plexus or peripheral nerve injury that failed to heal spontaneously and require surgical treatment. 4. Patients with obvious muscle atrophy suspected of brachial plexus nerve injury who need surgical exploration and treatment. 5. Patients with suspected brachial plexus nerve injury who have a history of brachial plexus nerve injury with long-term pain affecting quality of life, ineffective conservative treatment, and are scheduled for brachial plexus neurolysis to relieve pain. 6. Patients with mild brachial plexus injury who have not fully recovered after rehabilitation and require further brachial plexus neurolysis. Patients who meet one of the above criteria, have no disturbance of consciousness, voluntarily sign the informed consent form and participate in this study, with no age restriction.

Exclusion criteria

Exclusion criteria: 1. Patients with concurrent neuritis; 2. Patients who have not undergone brachial plexus nerve surgery; 3. Patients with disturbance of consciousness; 4. Patients who are unwilling to sign the informed consent form and participate in this study; 5. Patients with a history of allergy to contrast agents; 6. Pregnant or lactating women; 7. Patients with concurrent severe cardiopulmonary dysfunction; 8. Pediatric patients under 18 years old. Contrast-enhanced ultrasound is prohibited for the above groups to ensure the safety of subjects and reduce potential adverse reactions.

Design outcomes

Primary

MeasureTime frame
Consistency evaluation;sensitivity;specificity;accuracy;positive predictive value;negative predictive value;

Secondary

MeasureTime frame
The incidence of adverse events and serious adverse events;

Countries

China

Contacts

Public ContactDing Yueyue

Jing'an District Central Hospital of Shanghai

dyyqd79@hotmail.com+86 21 61578000

Outcome results

None listed

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