Actively Recruiting

Age: 18Years - 75Years
All Genders
Healthy Volunteers
ID06615622

A Comparative Study of Peripheral Nerve Ultrasound Findings in Immune Mediated Peripheral Nerve Disorders; a Hospital-based Study

Led by Assiut University · Updated on 2025-10-03

90

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the use of neuromuscular ultrasound (NMUS), a non-invasive diagnostic tool, in patients with Guillain Barré Syndrome (GBS) and Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP). The study aims to see if nerve changes detected by ultrasound correspond to traditional electrodiagnostic tests and whether this method can help with early diagnosis, predict outcomes, and distinguish between different disease subtypes. Understanding these nerve alterations may improve diagnosis and patient care by revealing more about the disease progression and nerve damage. The study includes two groups: patients diagnosed with immune-mediated peripheral nerve disorders (GBS or CIDP) and healthy individuals as controls. Participants will undergo serial nerve ultrasounds and nerve conduction studies (NCS) over a six-month period to observe nerve morphology, monitor changes, and assess recovery predictions. The study also compares findings between patient and healthy groups to better understand nerve alterations in these conditions. Participants will be involved in multiple assessments during the six months, including nerve ultrasound imaging and clinical evaluations. Researchers will measure nerve changes, correlate these with clinical scales, and track disease subtype distinctions. The study will monitor nerve alterations over time and compare them with healthy controls to identify meaningful differences. The total participation period is six months, during which safety and disease progression will be closely observed.

CONDITIONS

Brief Title

Our Study Aims to Determine if Nerve Alterations in Acute GBS and CIDP Detectable by Ultrasound Match Electrodiagnostic Findings and if This Method Aids Early Diagnosis, Predict Their Outcomes and Differentiate Between Axonal and Demyelinating Subtypes.

Who Can Participate

Age: 18Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Guillain Barré Syndrome according to NINDS and Brighton Collaboration (2011) criteria or CIDP according to EFNS/PNS criteria
  • Age between 18 and 75 years
  • Recent onset of GBS within first 2 weeks of symptoms or relapsing/progressive CIDP
  • Both males and females eligible
  • Willingness to participate and undergo study assessments
  • Ability and willingness to provide informed consent
Not Eligible

You will not qualify if you...

  • Unable or unwilling to provide informed consent
  • Presence of metabolic disorders or malignancies
  • Other causes of peripheral neuropathy
  • Other causes of acute flaccid paralysis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 2 weeks

Participants undergo peripheral nerve ultrasound and electrodiagnostic assessments to detect nerve alterations and assist early diagnosis.

1 to 2 visits depending on diagnostic assessments

Long-term Monitoring

Duration - 6 months

Participants are monitored over time to evaluate nerve morphology evolution, predict outcomes, differentiate subtypes, and correlate findings with clinical scales.

Periodic visits over 6 months

Trial Site Locations

Total: 1 location

1

Assiut University Hospitals

Asyut, Egypt

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Research Team

M

Mohammed Gad Ibrahim, MB, BCh

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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