CompletedMS (type not specified)NCT00819000

What it found

Result in a paper, not read yet

A paper reports the results; we have not read it yet. See Papers below.

What was tested

Treatment tested

What it measured

Main measures

  • Relationship of therapy Medication Possession Ratio (MPR), to patient outcomes

    12 months and 24 months

Other measures (1)

  • Relationship of therapy adherence, defined as the accumulation of time from initiation to discontinuation of therapy and measured by time, to patient outcomes

    12 months and 24 months

    Quality of life (reported by participants)

Who could take part

MS (type not specified) · 18 and over

Inclusion Criteria: * Male or female, 18 years of age or older, with a diagnosis of MS. * Being treated with Glatiramer Acetate (GA) or (IFN)-β * Receiving therapy from a participating Specialty Pharmacy Exclusion Criteria: * Has any contraindication to GA or IFN-β therapy, including pregnancy, trying to become pregnant, or breast feeding during the study * Has received an experimental drug in the last thirty (30) days other than Fampridine SR (4-aminopyridine or 4-AP) * Unlikely to be able to participate for the full two years of the study

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

The purpose of this study is to determine if higher compliance and adherence rates to drug therapy for MS result in better health outcomes than lower rates of therapy compliance and adherence.

Papers

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Related trials

History

    1. Started

      Dec 2008

    2. Main results due

      Dec 2012

    3. Finished

      Jan 2013

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