Could your own belly fat help fight MS?
NCT ID NCT03461419
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether a patient's own fat cells, processed into a special mixture called stromal vascular fraction, can safely improve quality of life and slow nerve damage in multiple sclerosis. About 100 adults with stable MS who have lasting nerve problems will receive an IV infusion of their own cells. The trial is currently suspended, and it is too early to know if this approach works.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- autologous adipose-derived cellular stromal vascular fraction (AD-cSVF)
- What this could lead to
- If it works, this could point toward a new way to manage multiple sclerosis by using the body's own cells to calm the immune system.
- What could go wrong
- The trial is suspended and early-stage, with no phase assigned. It is small (100 people) and uses a complex procedure that may not show clear benefit or could cause side effects.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2019
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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 to 85 years
- 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: * Documented functional damage to central or peripheral nervous system unlikely to improve with present standard of care * At least 6 months after onset of disease process * If under current medical therapy (drug or surgical) for the condition, patient considered stable on that treatment and unlikely to have significant reversal of associated neurological functions damage as a result of ongoing treatments * In estimation of providers and neurologists have the potential for improvement with AD-cSVF treatment, and be at minimal risk of potential harm from the procedure * Over 18 year old, and capable of providing informed consent * Medically stable and cleared by primary care physician, neurologist, or licensed practitioner that patient is felt to be reasonably expected to be expected to undergo procedures without known significant risk to health Exclusion Criteria: * Patient must be capable of an adequate neurologic examination and evaluation to document the pathology and ability to cooperate with examination * Patient must be capable and willing to undergo follow up neurologic exams with investigators or their own neurologists * Patient must be capable and competent to provide informed consent to participation * In estimation of investigators, the patient may be at increased or significant risk of harm to the patient's general health or neurologic functions for collection of AD-cSVF collection * Patients not medically stable, or who may be at significant risk to their health undergoing any and all procedures will not be eligible * Women of childbearing age must not be pregnant at the time of treatment, and should refrain from becoming pregnant for 3 months post-treatment
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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
2 sites in 2 countries. 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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Global Alliance of Regenerative Medicine (GARM) International
Roatán, Hn, Honduras, Honduras
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Robert W. Alexander, MD, FICS, LLC
Stevensville, Montana, 59870, United States
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