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Completed

NCT Number: NCT01847287

A Longitudinal Study of Brain Atrophy in MS Patients Over 5 Years

The primary aim of this study is to evaluate the effect of using Tysabri on changes in the brain using MRI and on disease progression in patients with relapsing-remitting Multiple Sclerosis over 5 years.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Buffalo Neuroimaging Analysis Center

Buffalo, New York, 14203, United States

About this study

This is a prospective, observational, single-blinded, longitudinal study of natalizumab effect on brain atrophy development and disability progression in multiple sclerosis patients over 5 years, which will evaluate originally treated patients with natalizumab who participated in a prospective 1- and 2-year VWMTR study. (Zivadinov et al., 2011b) All subjects will be assessed at 5-year follow-up with the same clinical examinations and will obtain 1.5T MRI examination on the same scanner that did not undergo any upgrade changes in the period of 5 years.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participation in natalizumab 1-year follow-up study
  • Participants were aged 18-65
  • Have clinically definite MS according to the Polman criteria of either RR or RSP disease type
  • EDSS scores ≤6.5
  • disease duration <30 years
  • normal kidney function (creatinine clearance >59 mL/min)
  • started therapy either with natalizumab or IM interferon beta-1a (IFNβ-1a)
  • Signed informed consent
  • Normal kidney functioning (creatinine clearance >59)
  • None of the exclusion criteria

Exclusion criteria

  • A clinically significant infectious illness (e.g., cellulitis, abscess, pneumonia, septicemia) within 30 days prior to 5-year follow-up visit
  • Nursing mothers or pregnant women who will need to undergo 5-year follow-up MRI
  • Unwillingness or inability to comply with the requirements of this protocol including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to comply with the study protocol
  • Any other reasons that, in the opinion of the Investigator, indicate that the subject is unsuitable for enrollment into this study

Treatment and study plan

Primary outcomes

  1. The primary aim of this study is to define the effect of the number of natalizumab cycles on development of brain atrophy and progression of disability in originally treated patients with natalizumab in relapsing multiple sclerosis (MS).

    Time frame: 5 years

    Evaluation of MRI images from baseline in comparison with a 5 year MRI.

Secondary outcomes

  1. The secondary objective of this study is to define the effect of the number of natalizumab cycles on accumulation of T2-LV and T1-LV and their VW-MTR changes over 5 years.

    Time frame: 5 years

    To evaluate any effect of the number of Tysabri cycles on lesion volume.

Sponsors and collaborators

Lead sponsor

University at Buffalo

Other

Registry information

Official study title

A Prospective, Observational, Single-blinded, Longitudinal Study of Natalizumab Effect on Brain Atrophy and Disability in Multiple Sclerosis Patients Over 5 Years.

Acronym: TST

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
May 6, 2013
Registry last updated
May 7, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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