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Brachial Plexus InjurySoana-ibpNCT06901063

Research of Brachial Plexus Anatomy

An observational study of Brachial Plexus Injury and Ultrasound, run by Huashan Hospital at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The research aims at analyzing the sonographic anatomy characteristics of the interscalene brachial plexus. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Brachial Plexus Injury, Ultrasound
What is being tested?
ultrasound
Type of treatment
Medical device
How many people
200 participants
Where
1 siteChina
Study dates
1 Apr 2025to 20 Jan 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Retrospectively collect ultrasound video of interscalene brachial plexus from existed departmental database.

Who may be able to join

  • ASA physical status class I or II
  • Scheduled for elective surgery

Who cannot join

  • Skin lesion or infection of neck
  • Any known peripheral neuropathy
  • Brachial nerve plexus injury
  • Previous injury or operation on neck
  • Pregnancy or breast feeding
  • Allergic to ultrasound gel

Trial locations and contacts

1 site in 1 country.

China1 site
  • Huashan Hospital Fudan University

    Shanghai, Shanghai Municipality, 200040

Other trials in China

About this study

Official title: Research of the Sonographic Anatomy of Interscalene Brachial Plexus

The research aims at analyzing the sonographic anatomy characteristics of the interscalene brachial plexus.

Being tested
ultrasound
Keywords
Brachial plexus, Nerve block, Ultrasound

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ultrasoundDevice

    Using ultrasound probe to scan and record the bilateral interscalene brachial plexus

Study groups in NCT06901063
Study groupRoleWhat they receive
The study groupThe recruited patients will be included in this group
Receives: Device: ultrasound

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The distribution of the number of visible bundles in C6 nerve root

    The percentage of one, two and multiple nerve bundles which composing the C6 nerve root

    Measured: immediately after the procedure

Secondary outcomes (2)
  1. The distribution of the number of visible bundles in C5 nerve root

    The percentage of one, two and multiple nerve bundles which composing the C5 nerve root

    Measured: immediately after the procedure

  2. The distribution of the number of visible bundles in C7 nerve root

    The percentage of one, two and multiple nerve bundles which composing the C7 nerve root

    Measured: immediately after the procedure

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Mar 2025
  2. Study start1 Apr 2025
  3. Primary completion30 Dec 2025
  4. Study completion20 Jan 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Retrospective
Enrolment
200 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06901063
Sponsor's protocol ID
2025-yxy-1
Acronym
Soana-ibp
Status last verified
Feb 2026
First submitted
23 Mar 2025
Last updated
10 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Brachial Plexus Injury and Ultrasound, run by Huashan Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The distribution of the number of visible bundles in C6 nerve root (time frame: immediately after the procedure). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Feb 2026.

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