Tears may replace spinal taps for MS diagnosis
NCT ID NCT02016222
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether a tear sample can diagnose primary progressive multiple sclerosis (MS) as accurately as a spinal tap. Currently, doctors need to collect spinal fluid to confirm this type of MS, which is invasive and uncomfortable. Researchers will compare proteins in tears and spinal fluid from 80 adults with progressive MS to see if tears can serve as a reliable alternative.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple, non-invasive tear test to diagnose primary progressive multiple sclerosis, avoiding the need for a spinal tap.
- What could go wrong
- This is an early-stage study with only 80 participants, so results may not apply to everyone. The tear test might not be accurate enough to replace the standard spinal fluid analysis.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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80 people
The number who actually took part.
- Start date
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Apr 2011
- Finished
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Mar 2016
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 18 years old or more * Progressive neurological deficit after 12 months * At least 9 T2 brain lesions of minimum 3 mm evidenced by MRI and/or four or more T2 lesions of minimum 3 mm with positive Visual Evoked Potential and/or positive spinal cord MRI (at least two focal T2 lesions) Exclusion Criteria: * Asiatic persons * recurrent forms of the disease * Persons wearing contact lenses * Ocular Infection * Corticoid treatment at least 30 days before sampling * immunosuppressive or immunomodulatory treatment 3 months before sampling
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Assistance Publique - Hôpitaux de Marseille
Marseille, 13354, France
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Centre hospitalier intercommunal
Poissy, 78303, France
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Centre hospitalier régional universitaire
Clermont-Ferrand, 63003, France
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Centre hospitalier régional universitaire
Lille, 59037, France
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Centre hospitalier régional universtaire
Strasbourg, 67091, France
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Centre hospitalier universitaire
Caen, 14033, France
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Centre hospitalier universitaire
Dijon, 21079, France
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Centre hospitalier universitaire
Nancy, 54035, France
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Centre hospitalier universitaire
Nîmes, 30029, France
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Centre hospitalier universitaire (CHU), Nice
Nice, Alpes Maritimes, 06003, France
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Centre hospitaliere universitaire
Bordeaux, 33404, France
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Groupement des Hôpitaux de l'Institut Catholique de Lille (GHICL)
Lille, Nord, 59000, France
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Hospices civils de Lyon
Lyon, 69229, France
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Other studies related to the condition(s) this trial covers.
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- Can a blood pressure pill slow MS disability?
- Could a simple injection replace an IV for MS treatment?
- Could a common supplement fight fatigue in progressive MS?
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