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A Multicentre randomiSed Controlled TRial of IntraVEnous Immunoglobulin Versus Standard Therapy for Transverse Myelitis

Phase 3
Terminated
Conditions
Myelitis, Transverse
Neuromyelitis Optica
Interventions
Registration Number
NCT02398994
Lead Sponsor
Guy's and St Thomas' NHS Foundation Trust
Brief Summary

This multi-center randomized controlled trial evaluates if the addition of intravenous immunoglobulin to standard treatment of corticosteroids improves outcome in children and adults with first episode of Transverse Myelitis of Neuro-myelitis optica. Half of participants will receive corticosteroids alone, whilst the other half will receive corticosteroids plus intravenous immunoglobulin.

Detailed Description

Transverse myelitis (TM) is a severe demyelinating condition predominantly affecting young people, which causes significant long-term disability in approximately one third. Current initial treatment is with corticosteroids, although evidence for their use is based on extrapolation from trials in adult multiple sclerosis relapses. In view of the severity of the condition, additional treatments have been trialed.

Intravenous immunoglobulin (IVIG) is often used as second-line treatment in steroid-unresponsive central nervous system demyelination, although evidence for its efficacy is limited to small case series and case reports. Randomized controlled trials have demonstrated that IVIG reduces inflammation and enhances remyelination in a number of neurological conditions, although there have been no randomized controlled trials testing its use in adults and children with TM.

This study will evaluate if additional and early treatment with IVIG is of extra benefit in TM when compared to the current standard therapy of intravenous steroids alone.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
2
Inclusion Criteria
  • Diagnosis of

EITHER acute first onset transverse myelitis (using the TM Consortium Working Group 2002 criteria) - patients must fulfill all of the following criteria:

  • Sensory, motor, or autonomic dysfunction attributable to spinal cord disease
  • Bilateral signs and/or symptoms (not necessarily symmetric)
  • Sensory level (except in young children <5 years where this is difficult to evaluate)
  • Lack of MRI brain criteria consistent with multiple sclerosis
  • Progression to nadir between 4 h and 21 days

OR first presentation of neuromyelitis optica (using standardised criteria) - patients must fulfil both absolute criteria:

  • Optic neuritis

  • Acute myelitis, plus two out of three supportive criteria (as Aquaporin 4 antibody (AQP4) is often not available acutely, only the first two supportive criteria would be applied),

  • Brain MRI not meeting criteria for Multiple Sclerosis (MS) at disease onset

  • Spinal cord MRI with contiguous T2-weighted signal abnormality extending over three or more vertebral segments, indicating a relatively large lesion in the spinal cord

  • AQP4 seropositive status

    • ASIA Impairment Score of A-C
    • Randomisation to occur no later than day 5 of steroids, and, if definitely known, within 21 days from symptom onset.
    • Give assent (8-16 years)/consent to participate in the trial
Exclusion Criteria
  • Contraindication to IVIG as stated in the summary of product characteristics (SmPC), or receiving IVIG for other reasons
  • Previously known systemic autoimmune disease (e.g. systemic lupus erythematosus) or any evidence of systemic inflammation during current presentation.
  • Direct infectious aetiology (e.g. varicella zoster)
  • Previous episode of central nervous system (CNS) inflammatory demyelination
  • Acute disseminated encephalomyelitis (ADEM)
  • Other causes of myelopathy not thought to be due to myelitis (e.g. nutritional, ischaemic, tumour etc.)
  • Other disease which would interfere with assessment of outcome measures
  • Known pregnancy
  • Circumstances which would prevent follow-up for 12 month

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intravenous MethylprednisoloneIntravenous MethylprednisolonePaediatric patients - 30mg/kg or 500mg/m2 up to a maximum daily dose of 1g/day for 5 days. Adult patients - 1g/day for 5 days.
Intravenous ImmunoglobulinIntravenous ImmunoglobulinPaediatric patients \<41.2kg - total dose of 2g/kg in divided doses over 2 days. All other patients - total dose of 2g/kg in divided doses over 5 days. PLUS Intravenous Methylprednisolone Pediatric patients - 30mg/kg or 500mg/m2 up to a maximum daily dose of 1g/day for 5 days. Adult patients - 1g/day for 5 days.
Intravenous ImmunoglobulinIntravenous MethylprednisolonePaediatric patients \<41.2kg - total dose of 2g/kg in divided doses over 2 days. All other patients - total dose of 2g/kg in divided doses over 5 days. PLUS Intravenous Methylprednisolone Pediatric patients - 30mg/kg or 500mg/m2 up to a maximum daily dose of 1g/day for 5 days. Adult patients - 1g/day for 5 days.
Primary Outcome Measures
NameTimeMethod
2 points or greater improvement on the American Spinal Injury Association (ASIA) Impairment scale (classified A-E)6 months
Secondary Outcome Measures
NameTimeMethod
Client Service Receipt Inventory (CSRI)6 months
Change in Kurtzke's expanded disability status scale (EDSS) measured with Neurostatus scoring6 months
Change in ASIA motor scale (0-100) and ASIA sensory scale (0-112)6 months
EQ-5D-5L (for patients aged 13 years or over at presentation)6 months
International Spinal Cord Injury (SCI) Quality of Life Basic Data Set (for patients aged 13 years or over at presentation)6 months
EQ-5D-Y (for patients aged 8-12 years at presentation)6 months

Trial Locations

Locations (18)

University Hospital Bristol NHS Foundation Trust

🇬🇧

Bristol, United Kingdom

University Hospitals Birmingham NHS Foundation Trust

🇬🇧

Birmingham, United Kingdom

Cardiff and Vale University Health Board

🇬🇧

Cardiff, United Kingdom

Birmingham Children's Hospital NHS Foundation Trust

🇬🇧

Birmingham, United Kingdom

North Bristol NHS Trust

🇬🇧

Bristol, United Kingdom

Great Ormond Street Children's Hospital

🇬🇧

London, United Kingdom

Walton Centre NHS Foundation Trust

🇬🇧

Liverpool, United Kingdom

King's College Hospital NHS Foundation Trust

🇬🇧

London, United Kingdom

University of London and Bart's Health NHS Trust

🇬🇧

London, United Kingdom

Central Manchester University Hospitals NHS Foundation Trust

🇬🇧

Manchester, United Kingdom

NHS Lothian

🇬🇧

Edinburgh, United Kingdom

Alder Hey Children's NHS Foundation Trust

🇬🇧

Liverpool, United Kingdom

Newcastle-upon-Tyne Hospitals NHS Trust

🇬🇧

Newcastle, United Kingdom

Nottingham University Hospitals NHS Trust

🇬🇧

Nottingham, United Kingdom

University Southampton NHS Foundation Trust

🇬🇧

Southampton, United Kingdom

Salford Royal NHS Foundation Trust

🇬🇧

Salford, United Kingdom

Oxford University Hospitals NHS Trust

🇬🇧

Oxford, United Kingdom

Guy's and St Thomas' NHS Foundation Trust

🇬🇧

London, United Kingdom

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