Post-Authorization Observational Study to Evaluate Cognition and Fatigue in Relapsing-remitting Multiple Sclerosis (RRMS) Patients Treated With Rebif®
Information source: Merck KGaA
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Multiple Sclerosis, Relapsing-Remitting
Intervention: Rebif (Interferon beta-1a) (Drug)
Phase: N/A
Status: Completed
Sponsored by: Merck KGaA Official(s) and/or principal investigator(s): Medical Responsible, Study Director, Affiliation: Merck spol.s.r.o., Czech Republic
Summary
The study is planned to evaluate the cognitive functions in subjects with RRMS treated with
interferon beta-1a, and its relationship to the fatigue and neurological dysfunction status.
Clinical Details
Official title: Post-Authorization Observational Study to Evaluate Cognition and Fatigue in RRMS Patients Treated With Rebif
Study design: Observational Model: Cohort, Time Perspective: Prospective
Primary outcome: Percentage of subjects with decreased/increased/stable cognition status (PASAT)
Secondary outcome: Percentage of subjects with decreased/increased/stable fatigue (FDS)Relationship between the cognition status, the fatigue status and the EDSS status Relationship between the Rebif dosage used with cognition and fatigue status Proportion of relapse-free subjects Proportion of subjects with defined EDSS changes (decrease; no change; increase of 0.5 - 1.0; 1.5 - 2.0; 2.5 - 3.0; 3.0 or more points, respectively) Proportion of subjects without either relapse, EDSS progression, cognition status decrease and fatigue increase Number of Rebif doses not taken since the last study visit, and the reason of dose not taken Proportion of subjects using the antidepressive or antifatigue medication
Detailed description:
Besides the motor and sensory dysfunctions, the progression of cognitive decline is a
frequent manifestation of RRMS. Fatigue is another important symptom of MS, and can
negatively affect subject's Quality of life (QoL) and socio-economic functioning, including
the ability to work, independent of the direct effects of disability. This is a phase IV
observational, non-interventional, prospective, multicentric study to evaluate cognition in
RRMS subjects treated with Rebif and its relationship to the fatigue and neurological
dysfunction status. The study plans to enroll 300 subjects, across 14 centres in Czech
Republic, who will be prescribed with Rebif according to its summary of product
characteristics (SmPC). Assessment of cognitive and fatigue status will be done at baseline
and follow-up visits at Months 3, 6, 12, 24. Subjects will be selected using the convenience
method following the non-probability sampling.
OBJECTIVES
Primary Objective:
- To assess changes of cognition [measured by Paced Auditory Serial Addition Test
(PASAT)] in RRMS subjects treated with Rebif
Secondary Objectives:
- To assess changes of fatigue [measured by Fatigue Descriptive Scale (FDS)] in RRMS
subjects treated with Rebif
- To assess a correlation between cognition, fatigue and neurological status in RRMS
subjects treated with Rebif
- To assess a relationship between Rebif dosage [22 mcg vs 44 mcg thrice a week (tiw)]
and cognition (PASAT)
- To assess a relationship between Rebif dosage (22 mcg vs 44 mcg tiw) and fatigue (FDS)
- To assess adherence to Rebif treatment
- To explore the use of antidepressive and antifatigue medicaments
Eligibility
Minimum age: 18 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Subjects diagnosed with RRMS
- Subjects eligible for treatment with Rebif as per SmPC, the Czech local guidelines
and the actual Health insurance policy.
- Subjects 18-65 years of age
- Subjects with EDSS score < 4
- Subjects who are willing and able to give informed consent
Exclusion Criteria:
- Treatment with Rebif for more than 24 months prior the informed consent form has been
obtained.
- Subjects with history of hypersensitivity to natural or recombinant interferon-β, or
to any excipients
- Female subject who is pregnant or breast feeding and/or planning to become pregnant
- Subjects with current severe depression and/or suicidal ideation
- Any contraindication for Rebif therapy as per SmPC
- Subjects with severe disability and/or any neurologic or psychiatric condition that
may interfere with test performance
- Prior treatment with interferon beta-1a i. m. or interferon beta-1b or glatiramer
acetate.
Locations and Contacts
Neurologicka klinika FNBB, Brno, Czech Republic
Neurologicka klinika, Fakultní nemocnice U Sv. Anny, Brno, Czech Republic
Neurologicke oddeleni KN., Ceske Budejovice, Czech Republic
Neurologicka klinika Fakultní nemocnice, Hradec Kralove, Czech Republic
Neurologicka klinika Fakultní nemocnice, Motol, Czech Republic
Neurologicka klinika, Fakultní nemocnice, Olomouc, Czech Republic
Neurologicka klinika Fakultní nemocnice, Ostrava, Czech Republic
Neurologicke oddeleni KN, Pardubice, Czech Republic
Neurologicka klinika Fakultní nemocnice, Plzeň, Czech Republic
Neurologicka klinika FNKV, Praha, Czech Republic
Neurologicka klinika, Fakultní Thomayerovy nemocnice, Praha, Czech Republic
Neurologicke oddeleni NsP, Teplice, Czech Republic
Neurologicke oddeleni, Baťova nemocnice, Zlín, Czech Republic
Additional Information
Starting date: May 2009
Last updated: September 5, 2013
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