Correlation Between Multiple Sclerosis Functional Composite (MSFC) and Expanded Disability Status Scale (EDSS) in Patients With Multiple Sclerosis (MS) in Argentina

NCT ID: NCT01080014

Last Updated: 2013-10-16

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 252 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2008-08-31
• Study Completion Date: 2013-04-30

Brief Summary

This observational study is being conducted to evaluate the usefulness of the MSFC and its relationship with EDSS scores in subjects with MS in Argentina.

Detailed Description

This observational, open-label study is being conducted to correlate change in EDSS score with the change in MSFC scores at the end of a 2-year follow-up period for subjects with MS in Argentina. Measurement of disability is an indispensable parameter in assessing the efficacy of experimental therapeutic agents in MS as well as in trying to determine possible individual evolution of the disease. Clinical scales are being used as primary or secondary outcome measures for recording disease progression in clinical trials. Kurtzke's EDSS is still used as a gold standard for measuring impairment and disability in MS. The MSFC is an examination-based quantitative scoring of neurological impairment. This study aims to establish a correlation between the usefulness of both scales.

OBJECTIVES

Primary Objective:

• To evaluate the change in MSFC score with change in EDSS scores at end of 2 year follow-up period for subjects with MS in Argentina

Secondary Objectives:

• To evaluate the cross-sectional correlations in MSFC score at baseline and at 24 months with EDSS score at baseline and at 24 months
• To describe the MSFC score for MS phenotype in this population
• To evaluate the predictive validity of MSFC score of a subsequent EDSS change in a subgroup of MS patients in Argentina

Conditions

Multiple Sclerosis

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Subjects with definite diagnosis of MS, according to McDonald's criteria
• All clinical types: relapsing-remitting MS (RRMS), primary progressive MS (PPMS) and secondary progressive MS (SPMS). Stable disease course without any relapse for at least the previous 3 months
• Subjects treated or not with disease modifying drugs
• Ages between 18 and 65 years and is capable of understanding and complying with protocol requirements
• Subject has a stable residence with no planned move during the entire investigation period

Exclusion Criteria

• Life expectancy less than 5 years at admission
• Diagnosis of clinically isolated syndrome (CIS)
• Other clinical conditions that mimic MS
• Psychiatric diseases
• Alcohol or drug abuse
• Pregnancy
• The subject is unwilling or unable to comply with the protocol or scheduled appointments
• Subject is unable to understand the language in which the approved informed consent is written
• The subject is a study site employee, or an immediate family member (i.e., spouse, parent, child, sibling) of a study site employee, involved in conduct of this study

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Merck KGaA, Darmstadt, Germany

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dr. Roberto Rosa, PhD

Role: PRINCIPAL_INVESTIGATOR

PhD Neurologist, Unaffiliated

Locations

Dr. Roberto Rosa

Buenos Aires, , Argentina

Countries

Argentina

Other Identifiers

EMR 200077_502

Identifier Type: -

Identifier Source: org_study_id