Multiple Sclerosis Trial, Recruiting NCT06369766 Sponsor: University Hospital, Basel, Switzerland Condition: Multiple Sclerosis
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Multiple Sclerosis Trial, Recruiting

NCT06369766
Recruiting Not Applicable

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 older than 18 years of age
  • People who have been diagnosed with Multiple Sclerosis, based on the 2017 McDonald Criteria
  • People who have been diagnosed with Neuromyelitis Optica Spectrum Disorder, Myelin Oligodendrocyte Glycoprotein Antibody Disease, or another neuroinflammatory condition other than Multiple Sclerosis

Who may not be able to join:

  • People who are unable to have a specific eye scan called Optical Coherence Tomography (OCT) or retinal vessel imaging — for example, due to severe uncontrolled eye movement that prevents focusing with both eyes
  • People who have an existing eye condition that could affect the reliability of the eye scan results, such as cataracts, glaucoma, or a history of significant vision correction needs above a certain level (confirm with trial site)
  • People who are currently pregnant or breastfeeding
  • Healthy volunteers who have a history of significant neurological conditions — such as stroke, certain inflammatory brain conditions, or nerve disorders — that could affect how results are assessed or interpreted

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Athina Papadopoulou, PD Dr. med., University Hospital Basel, Department of Neurology

Phone: +41 61 32 85704

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

Status
Recruiting
Phase
Not Applicable
Sponsor
University Hospital, Basel, Switzerland
Registry
ClinicalTrials.gov
Start date
31 January 2024
Est. completion
1 December 2028

Where this trial is recruiting

🇨🇭 Switzerland

Primary endpoints

Occurence of Progression Independent of Relapse Activity (PIRA); Neuroaxonal loss in the retina (as marker of neurodegeneration in the CNS); Neuroinflammation in the retina; Fixation instability (as marker of global neuronal dysfunction in the CNS); Structural changes of the retinal vessels (as marker of systemic microvascular health); (For a subgroup of participants) Functional/perfusional changes of the retinal vessels

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov