Antioxidant supplement NAC tested for MS brain health
NCT ID NCT03032601
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests whether N-acetyl cysteine (NAC), a common antioxidant supplement, can improve brain function and reduce inflammation in people with multiple sclerosis (MS). Researchers will use brain scans to measure changes in metabolism and inflammation. The study enrolls 55 adults with MS who are not planning to start new medications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- N-acetyl cysteine (NAC)
- What this could lead to
- If it works, this could point toward a simple supplement to support brain health and reduce inflammation in multiple sclerosis.
- What could go wrong
- This is a small, early-stage study with no placebo control. NAC is generally safe, but benefits may be modest or not seen at all.
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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About 55 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2017
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- 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: * Clinical diagnosis of relapsing remitting MS or progressive MS who do not plan to start a medication during the study, or on stable disease modifying medication (interferon, glatiramer, dimethyl fumarate, teriflunomide). * Age 18 years old to no upper limit * Physically independent, ambulatory * Women of childbearing potential will confirm a negative pregnancy test and must practice effective contraception during the period of pilot study. In addition, male subjects who have a partner of childbearing age should practice effective contraception. * Participants must be able to complete study procedures in the greater Philadelphia area. Exclusion Criteria: * Patients are excluded who have received treatment with intravenous steroids within the past 90 days for reasons other than MS * Previous brain surgery that would interfere with determination of cerebral metabolism or structure on the FDG PET-MRI. * Score on Mini-Mental Status examination of 20 or lower. * Wheelchair-bound or bed-ridden, non-ambulatory. * Intracranial abnormalities that may complicate interpretation of the brain scans (e.g., stroke, tumor, vascular abnormality affecting the target area). * History of head trauma with loss of consciousness \> 48 hours. * History of asthma requiring daily medications for adequate management. * Any medical disorder or physical condition that could reasonably be expected to interfere with the assessment of MS symptoms, or with any of the study assessments including the PET-MRI imaging. * Patients with evidence of a significant psychiatric disorder by history/examination that would prevent completion of the study will not be allowed to participate. * Patients with current alcohol or drug abuse * Pregnant or lactating women. * Enrollment in active clinical trial/ experimental therapy within the prior 30 days. * Pending surgery during the course of the study. * Patients taking medications that might interact with NAC involved in this study will be evaluated on a case by case basis by the PI or study physician. These medications include: Medications for high blood pressure; Medications that slow blood clotting; Medications for diabetes; Nitroglycerin. * Patients with history of pulmonary hypertension. * Any neurological, psychiatric, or medical condition that might affect the distribution of the radiopharmaceutical in the body or brain (as determined by Investigator) * Currently using medications that might alter the distribution of radiopharmaceuticals in - -the body or brain (as determined by Investigator) * Patient exceeds the weight limit of the table * Claustrophobia that would prevent completion of imaging studies * Glucose level that would interfere with the FDG PET scan * Any additional contraindications for MRI; Has metallic objects (e.g., pacemakers) in the body
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
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