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November 1, 2006Multiple Sclerosis Journal

The MSBase registry, an international web platform for collaborative outcomes research in multiple sclerosis, has enrolled 2,400 patients across 11 countries.

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Key result

The MSBase registry, an international web platform for collaborative outcomes research in multiple sclerosis, has enrolled 2,400 patients across 11 countries.

Authors

HBHelmut ButzkuevenJCJoab ChapmanECEdgardo Cristiano

Discussion

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Overview

Enables multinational MS outcomes research; leaves open its impact on clinical decisions pending validation.

Study Design

Type

Cohort (n=2,400)

Multicenter

Yes

PICO

P
Population
2,400 patients with multiple sclerosis enrolled in an international, prospective observational registry across 11 countries.
E
Exposure / Comparator
MSBase registry

Cite This Study

Butzkueven et al. (2006) conducted a cohort in multiple sclerosis (n=2,400). MSBase registry was evaluated. The MSBase registry, an international web platform for collaborative outcomes research in multiple sclerosis, has enrolled 2,400 patients across 11 countries.

synapsesocial.com/papers/6a9be2d7c47b7d86ca68eacehttps://doi.org/10.1177/1352458506070775
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