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Study Comparing Corpus Callosum Atrophy as a Marker of Later Development of Cognitive Impairment in Patients With Multiple Sclerosis

Cohort Study Comparing Corpus Callosum Atrophy as a Marker of Later Development of Cognitive Impairment in Patients With Early and Remitting Relapsing Multiple Sclerosis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01250665
Enrollment
65
Registered
2010-12-01
Start date
2011-01-31
Completion date
2011-06-30
Last updated
2010-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Impairment, Multiple Sclerosis

Keywords

multiple sclerosis, cognitive impairment, interferon-beta 1b, corpus callosum index

Brief summary

This study is a cross sectional study of patients diagnosed with clinically isolated syndrome (CIS) and RRMS, who will undergo a series of tests to assess cognitive impairment, fatigue severity and depressive symptoms. Cognitive impairment will be assessed with Multiple Sclerosis Inventory Cognition (MUSIC) and symbol digit modalities test (SDMT), fatigue severity will be measured with the Fatigue Scale for Motor and Cognitive Functions (FSMC) and depressive symptoms with the Beck Depression Inventory (BDI). All tests mentioned above are validated for MS patients. In the second step we will use our large longitudinal database of serial MRI examinations from which a linear measurement of CCI will be retrospectively calculated.

Interventions

None listed

Sponsors

Bayer
CollaboratorINDUSTRY
Cantonal Hospital of St. Gallen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Patients between 18 and 55 years at presentation * Diagnosis of relapsing-remitting MS according to revised McDonald criteria 2005, clinically isolated syndrome suggestive of MS * Patients treated with interferon-beta 1b * Untreated patients * EDSS under 5.5

Exclusion criteria

* Brain pathology other than MS * Known history of head trauma * Pure spinal manifestation of demyelization * Neuromyelitis optica * Primary and secondary progressive MS * Benzodiazepine intake within the last three months * Relapse within the last three months * Steroid intake within the last three months * History of severe depressive disorder and/or suicidality, seizure, drug or alcohol abuse * No informed consent * Insufficient knowledge of German

Design outcomes

Primary

MeasureTime frameDescription
Multiple Sclerosis Inventory Cognition (MUSIC)MUSIC is a cognitive screening instrument. It assesses the cognitive core deficit in MS (mental flexibility, attention, information processing speed, memory and inhibitory control) and includes 3 items derived from a factorial analysis to examine cognitive, motor and psychosocial fatigue, respectively.
Annual Corpus Callosum Index decreaseCorpus callosum index (CCI) is an easy to use MRI marker for estimating brain atrophy in patients with MS. Demonstrated correlation of CCI and atrophy has been measured with brain parenchymal fraction.

Secondary

MeasureTime frameDescription
Corpus callosum Index at baselineThe CCI at baseline will be measured from MRI findings acquired at diagnosis of clinically isolated syndrome.
Time to clinically definite MSThis is the time in months then patients diagnosed with CIS go on to develop clinically definite MS (CDMS). CDMS will be diagnosed if patients fulfill the criteria for remitting relapsing MS according to Poser (Poser 1983) or McDonald (McDonald 2001).
The Symbol Digit Modalities Test (SDMT)SDMT is an easily administered brief cognitive performance tests. This test emphasizes working memory and speed processing.
Ratio treatment duration to disease durationThe ratio of duration of treatment (DT) to duration of disease (DD): DT/DD. Duration of treatment is the cumulative time of treatment with interferon-beta 1b. Duration of disease starts from the first presentation of MS symptoms

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026