Evidence map›Paper›PMID 42081777›Full record

Trial reportNeurology2026

Intrathecal Mesenchymal Stem Cells in Progressive Multiple Sclerosis: A Randomized, Double-Blind, Placebo-Controlled Trial (SMART-MS).

Christopher Elnan Kvistad, Torbjørn Kråkenes, Trygve Holmøy, Live Egeland Eidem, Linn Steffensen, Kristin Wesnes, Markus Rojewski, Tom Eichele, Stig Wergeland, Sonia Gavasso and 15 more

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase IIClinical Trial, Phase I
In one paragraph

Trial report in Neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04749667 (Study of Mesenchymal Autologous Stem Cells as Regenerative Treatment for Multiple Sclerosis), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04749667 phase1 / phase2active not recruitingnot on this map

Study of Mesenchymal Autologous Stem Cells as Regenerative Treatment for Multiple Sclerosis

TypeinterventionalSponsorHaukeland University HospitalRan2021 to 2027Enrolled18ConditionsMultiple Sclerosis, Progressive Multiple SclerosisArmsMSCs, Saline
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Stem Cell-Based Therapies for Central Nervous System Demyelinating Diseases: Clinical Evidence, Therapeutic Niches, and Translational Boundaries.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Christopher Elnan KvistadDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-8393-2772
Torbjørn KråkenesDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.
Trygve HolmøyDepartment of Neurology, Akershus University Hospital, Lørenskog, Norway.ORCID 0000-0002-2529-5664
Live Egeland EidemResearch Department, Stavanger University Hospital, Norway.ORCID 0009-0005-2033-1864
Linn SteffensenDepartment of Neurology, University Hospital of North Norway (UNN), Tromsø, Norway.
Kristin WesnesDepartment of Neurology, St. Olavs Hospital, Trondheim, Norway.
Markus RojewskiInstitute of Transfusion Medicine, University of Ulm and Institute of Clinical Transfusion Medicine and Immunogenetics Ulm, Red Cross Blood Transfusion Service Baden-Württemberg-Hessen and University Hospital Ulm, Ulm, Germany.ORCID 0000-0003-4265-0442
Tom EicheleDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.
Stig WergelandDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-7645-7686
Sonia GavassoDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.
Harald BarsnesProteomics Unit, Department of Biomedicine, University of Bergen, Norway.
Jörg AssmusCentre for Clinical Research, Haukeland University Hospital, Bergen, Norway.
Niyaz Al-SharabiDepartment of Clinical Dentistry, University of Bergen, Norway.
Samih Mohamed-AhmedDepartment of Clinical Dentistry, University of Bergen, Norway.
Hugo VrenkenMS Center, Amsterdam, the Netherlands.ORCID 0000-0001-9106-1172
Iman BrouwerMS Center, Amsterdam, the Netherlands.ORCID 0000-0002-0408-0461
Henk-Jan Mm MutsaertsMS Center, Amsterdam, the Netherlands.ORCID 0000-0003-0894-0307
Mario TranfaMS Center, Amsterdam, the Netherlands.ORCID 0000-0002-4451-4746
Cecilie GjerdeDepartment of Clinical Dentistry, University of Bergen, Norway.
Marie YtterdalDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID 0009-0004-6032-7600
Eyvind RødahlDepartment of Clinical Medicine, University of Bergen, Norway.ORCID 0000-0003-1025-4840
Frode Steingrimsen BervenProteomics Unit, Department of Biomedicine, University of Bergen, Norway.
Hubert SchrezenmeierInstitute of Transfusion Medicine, University of Ulm and Institute of Clinical Transfusion Medicine and Immunogenetics Ulm, Red Cross Blood Transfusion Service Baden-Württemberg-Hessen and University Hospital Ulm, Ulm, Germany.
Kamal MustafaDepartment of Clinical Dentistry, University of Bergen, Norway.
Lars BøDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThere is an unmet need for neuroregenerative therapies in multiple sclerosis (MS). Mesenchymal stem cells (MSCs) have shown immunomodulatory and regenerative effects in preclinical models and early clinical studies. Intrathecal administration may enhance therapeutic potential by direct delivery to the CNS. However, randomized, placebo-controlled trials are needed to establish safety and efficacy. The objective of this trial was to assess whether a single intrathecal administration of autologous MSCs could provide evidence of a neuroregenerative effect in progressive MS.

methodsIn this randomized, double-blind, placebo-controlled phase I/II trial (NCT04749667), patients with progressive MS enrolled at 4 Norwegian tertiary hospitals received a single intrathecal injection of autologous bone marrow-derived MSCs (1 × 10

resultsA total of 18 patients were included (mean age 46.7 years; 55.6% female). No significant between-group difference was observed for the primary end point (β = -0.31, 95% CI -1.84 to 1.22, DISCUSSION: A neuroregenerative effect was not detected, although interpretation may be limited by the small sample size. Adverse events suggest an acute localized inflammatory reaction after MSC administration. Our findings suggest that intrathecal administration of MSCs in progressive MS should be approached with caution in future studies. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that, in patients with progressive multiple sclerosis, treatment with a single intrathecal administration of autologous mesenchymal stem cells does not provide neuroregenerative effect, as assessed by a composite evoked potential score.

trial registrationClinicalTrials.gov (NCT04749667); registered February 8, 2021; first patient enrolled August 9, 2021.

Indexed as

Mesenchymal Stem Cell TransplantationMultiple Sclerosis, Chronic ProgressiveAdultCross-Over StudiesDouble-Blind MethodFemaleHumansInjections, SpinalMagnetic Resonance ImagingMaleMiddle AgedTransplantation, AutologousTreatment Outcome

Identifiers

PMID42081777
PMCPMC13148372

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.