Peripheral Neuropathy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with Guillain-Barré Syndrome (GBS) according to recognised international diagnostic guidelines, or people diagnosed with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) according to European neurological society guidelines.
- People aged between 18 and 75 years old.
- For GBS: People whose symptoms started within the last 2 weeks. For CIDP: People whose condition either comes and goes in episodes, or is slowly getting worse over time.
- Both men and women are eligible to join.
- People who are willing to take part in study-related check-ups and assessments.
- People who are able to understand and willing to sign an informed consent form agreeing to take part.
Who may not be able to join:
- People who are unable or unwilling to sign an informed consent form.
- People who have metabolic disorders or any form of cancer.
- People whose nerve damage is caused by something other than GBS or CIDP.
- People whose muscle weakness or paralysis is caused by a condition other than GBS or CIDP.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +201022748859
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Detection of Nerve Alterations via Ultrasound
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.