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 are a close blood relative (parent, child, or sibling) of someone diagnosed with SPG4 or who carries a known mutation in the SPAST gene
- People aged 18 to 70 years
- People who are willing and able to provide written consent to participate
Who may not be able to join:
- People whose family does not have a confirmed SPAST gene mutation
- People who already show clear signs of spastic walking (some early physical signs, such as overactive reflexes or a positive Babinski reflex, may still be acceptable — confirm with trial site)
- People who are currently participating in another clinical trial that involves a medical intervention
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
Principal Investigator: Ludger Schöls, Prof., Head of Department
Phone: +49 7071 / 29
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
Identification of a change of recognizable signs or symptoms
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.