AI Cure is a research tool showing open data. Not medical advice. Discuss with your doctor. Terms

โ† Trials
๐Ÿงช

Retinal Neuro-vascular Coupling in Patients With Multiple Sclerosis

RecruitingNAAges 18 Years - anyAllMedical University of Vienna
๐Ÿ’ฌ

In plain words

What the trial is, and whether it could suit you

Multiple sclerosis (MS) affects approximately 2.3 million patients worldwide, with a global median prevalence of 33 per 100,000. MS is diagnosed at an average of 30 years and affects twice as many women as men. MS is traditionally diagnosed by the presentation of lesions of the central nervous system, disseminated in time and in space, proven by clinical examination and magnetic resonance imaging. Several anatomical parameters in the eye, both vascular and neural, have been found to be altered in MS patients. Because of its unique optical properties, the eye offers the possibility of the non-invasive assessment of both structural and functional alterations in neuronal tissue. As the neuro-retina is part of the brain, it does not come as a surprise that neuro-degenerative changes in the brain are accompanied by structural and possibly also functional changes in the neuro-retina and the o

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion criteria for healthy subjects: * Men and women aged over 18 years * Non-smokers * Normal findings in the medical history unless the investigator considers an abnormality to be clinically irrelevant * Normal ophthalmic findings, ametropy \< 6 Dpt. Inclusion criteria for patients with MS: * Men and women aged over 18 years * Diagnosis of relapsing-remitting multiple sclerosis (RRMS) according to clinical evaluation and McDonald criteria (revision 2010) * History of AON in one eye at least one year ago * Non-smokers * Normal ophthalmic findings, ametropy \< 6 Dpt. * Adequate visual acuity to allow participation in the ocular blood flow measurements * A potential participant has to be on stable doses of all medications he/she is taking because of consisting illnesses according to medical history (except MS therapy itself which will be recorded separately) for at least 30 days prior inclusion, if considered relevant by the investigator. Any of the following will exclude a healthy subject from the study: * Diagnosis of "possible MS" according to the McDonald criteria (revision 2010) * Presence or history of a severe medical condition as judged by the clinical investigator * Untreated Arterial hypertension * History or family history of epilepsy * Presence of any abnormalities preventing reliable measurements in the study eye as judged by the investigator * Family history of MS, optic neuritis, neuromyelitis optica (NMO, Devic disease) or NMO spectrum disorders * History of inflammatory or infectious disease of central nervous system * Best corrected visual acuity \< 0.5 Snellen * Ametropy โ‰ฅ 6Dpt * Pregnancy or planned pregnancy * Alcoholism or substance abuse Any of the following will exclude a patient from the study: * Presence or history of a severe medical condition other than MS as judged by the clinical investigator * History of neuromyelitis optica (NMO, Devic disease) or NMO spectrum disorders * History of inflammatory or infectious disease of central nervous system other than MS * Untreated Arterial hypertension * History or family history of epilepsy * Presence of any abnormalities preventing reliable measurements in the study eye as judged by the investigator * Best corrected visual acuity \< 0.5 Snellen * Ametropy โ‰ฅ 6 Dpt * Pregnancy, planned pregnancy * Significant neurological disease other than MS, if considered relevant by the investigator * Alcoholism or substance abuse
๐Ÿ’Š

What it tests

  • Dynamic Vessel Analyzer (DVA)
  • Fourier Domain Doppler Optical Coherence Tomography (FDOCT)
  • Optical coherence tomography (OCT)
  • Optical coherence tomography angiography (OCTA)
๐Ÿ“

Where

1 site
Department of Clinical Pharmacology, Medical University of Vienna
Vienna, Austria
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
๐Ÿ›ก๏ธ

AI Cure shows public evidence (Open Targets, ClinicalTrials.gov, PubMed, openFDA, DepMap, AlphaFold) with its source, and AI summaries that cite it โ€” not medical advice and not a cure. Treatment decisions belong with your doctor. Research ideas are shared only with approved researchers and labs, who can test them. In an emergency call your local emergency number (112 in India and Europe, 911 in the US). AI Cure Terms of Use ยท Privacy