Peripheral Nerve Ultrasound in Children With Guillain-Barré Syndrome

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-17
SponsorAssiut University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

- Age 1 to 17 years

Diagnosis compatible with Guillain-Barré syndrome according to Brighton criteria

Written informed consent from parent or legal guardian

Disqualifiers

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

Trial population

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

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

42 Participants
are grouped into 1 trial group
Group A: Children with Guillain-Barré Syndrome

Trial outcomes

Primary outcomes

1

Mean nerve cross-sectional area

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

Time frame
Baseline

Secondary outcomes

1

Change in nerve cross-sectional area

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

Time frame
At 3 months
2

Mean distal motor latency

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

Time frame
Baseline
3

Mean compound muscle action potential amplitude

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

Time frame
Baseline
4

GBS Disability Scale Score

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

Time frame
Baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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