CompletedMS (type not specified)NCT05141669

What it found

No result found

We found no results in the registry or in papers.

This trial finished 5 years ago. We found no results in the registry or in any paper that cites it.

What was tested

Treatment tested

What it measured

Main measures

  • Number of Multiple Sclerosis (MS) relapses

    Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)

    RelapsesQuality of life (reported by participants)

Other measures (5)

  • Number of Multiple Sclerosis-related inpatient admission

    Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)

    Quality of life (reported by participants)
  • Number of Multiple Sclerosis-related Emergency Room (ER) visits

    Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)

    Quality of life (reported by participants)
  • All-cause total (medical plus pharmacy) health care costs

    Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)

  • All-cause medical health care costs

    Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)

    Quality of life (reported by participants)
  • All-cause total (medical plus pharmacy) health care costs excluding fingolimod

    Month 7 to Month 18 (12 months) of the post-index period. The date of the first fingolimod claim was the index date (01 January 2012 through 10 May 2018)

    Quality of life (reported by participants)

Who could take part

MS (type not specified) · 18 to 85

Inclusion Criteria: * ≥18 years old during year of index date with valid gender and geographic information * Continuous enrollment (CE) in the health plan with medical and pharmacy benefits for ≥6 months (180ii days) before the index date (pre-index period) * CE with medical and pharmacy benefits for ≥18 months (540 days) beginning on the index date (post-index period) * All patients had uniform 6-month pre-index and 18-month post-index periods * ≥1 medical claim with an MS diagnosis codei in any position during the pre-or post-index periods * ≥1 claim for fingolimod after the index date (i.e., from index date +1 to 539 days post-index) * By requiring ≥1 medical claim with an MS diagnosis code and ≥2 claims with an NDC for fingolimod, the inclusion criteria essentially incorporated the preferred/overall best performing MS case-finding definition validated by Culpepper et al. The criteria for that definition required at least 3 separate encounters from any of the following: MS-related ambulatory visits, MS-related inpatient stays, and DMT claims during a 12-month period. Slightly higher accuracy was found when a 24-month period was used. Exclusion Criteria: •≥1 pharmacy or medical claim for any MS DMT during the pre-index period

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

About this trial

In the sponsor's words

This study was a retrospective observational claims data study of commercial and Medicare Advantage with Part D (MAPD) patients initiating fingolimod.

Loading reviews and guidelines…

Related trials

History

    1. Started

      May 2020

    2. Main results due

      Nov 2020

    3. Finished

      Nov 2020

    Assembled by software from public sources and not checked by people. Each record links to its source. Report an error