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Guillain-Barre SyndromeNCT07866898

Peripheral Nerve Ultrasound in Children With Guillain-Barré Syndrome

An observational study of Guillain-Barre Syndrome, run by Assiut University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

This prospective observational study aims to evaluate peripheral nerve ultrasound findings, particularly nerve cross-sectional area, in children with Guillain-Barré syndrome. Read more about this study

Who is it for?
Ages 1 year to 17 years
Conditions the study is for
Guillain-Barre Syndrome
How many people
42 participants
Where
No sites listed yet
Study dates
10 Oct 2026to 1 Feb 2028
Phase
Observational

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 1 year to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Study population: Children aged 1 to 17 years diagnosed with Guillain-Barré syndrome admitted to or evaluated at Assiut University Children's Hospital.

Who may be able to join

  • - Age 1 to 17 years
  • Diagnosis compatible with Guillain-Barré syndrome according to Brighton criteria
  • Written informed consent from parent or legal guardian

Who cannot join

  • Previous diagnosis of hereditary peripheral neuropathy
  • Chronic inflammatory demyelinating polyneuropathy or another chronic neuropathy
  • Previous neuromuscular disease affecting nerve conduction or ultrasound measurements
  • Significant peripheral nerve trauma or previous nerve surgery
  • Drug-induced neuropathy
  • Local anatomical abnormalities or marked edema preventing reliable ultrasound assessment

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Ahmed S Ahmed, Resident contact

+20 12 70363133

as99709@gmail.com

About this study

Official title: Diagnostic Value of Peripheral Nerve Ultrasound in Children With Guillain-Barré Syndrome

This prospective observational study aims to evaluate peripheral nerve ultrasound findings, particularly nerve cross-sectional area, in children with Guillain-Barré syndrome.

Read the detailed description

Guillain-Barré syndrome is an acute immune-mediated neuropathy. High-resolution peripheral nerve ultrasound can measure nerve cross-sectional area and detect structural abnormalities.

This observational study will perform peripheral nerve ultrasound and nerve conduction studies in children aged 1 to 17 years with Guillain-Barré syndrome at baseline and at 3 months.

Keywords
Guillain-Barre syndrome, Peripheral nerve ultrasound, Nerve cross-sectional area, Children, Assiut
Medical subject headings
Guillain-Barre Syndrome

What participants receive

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

Study groups in NCT07866898
Study groupRoleWhat they receive
Children with Guillain-Barré SyndromeChildren aged 1 to 17 years with Guillain-Barré syndrome undergoing peripheral nerve ultrasound and nerve conduction studies.

What is being measured

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

  1. Mean nerve cross-sectional area

    Mean cross-sectional area of selected peripheral nerves measured by high-resolution ultrasound in mm².

    Measured: Baseline

Secondary outcomes (4)
  1. Change in nerve cross-sectional area

    Mean change in peripheral nerve cross-sectional area in mm² from baseline to 3 months.

    Measured: At 3 months

  2. Mean distal motor latency

    Mean distal motor latency measured by nerve conduction study in milliseconds.

    Measured: Baseline

  3. Mean compound muscle action potential amplitude

    Mean compound muscle action potential amplitude measured by nerve conduction study in millivolts.

    Measured: Baseline

  4. GBS Disability Scale Score

    Mean Guillain-Barré Syndrome disability scale score (range 0 to 6, higher scores indicate worse disability).

    Measured: Baseline

Timeline

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

  1. First posted8 Oct 2026
  2. Study start10 Oct 2026 (estimated)
  3. Primary completion10 Oct 2027 (estimated)
  4. Study completion1 Feb 2028 (estimated)

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
Cohort
Time perspective
Prospective
Enrolment
42 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07866898
Sponsor's protocol ID
Nerve-US-GBS-Assiut-2026
Status last verified
Oct 2026
First submitted
5 Oct 2026
Last updated
8 Oct 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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