Multiple Sclerosis Clinical Trial

The Efficacy and Safety of Escitalopram for Depression in Multiple Sclerosis

Summary

Emotionally labile, depressed participants with multiple sclerosis treated with escitalopram will have a greater reduction in emotional lability scores and in their psychological distress scores than those who are randomized to receive placebo.

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Full Description

Patients with multiple sclerosis who are experiencing mood lability and symptoms of depression will be randomized to receive either escitalopram 10mg/day or placebo tablets for a period of 6 weeks. It is hypothesized that patients receiving medication will experience a greater normalization of their emotional instability and a greater reduction in their depressive symptoms at the end of the six-week trial than those who are not receiving medication.

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Eligibility Criteria

Inclusion Criteria:

Clinical diagnosis of multiple sclerosis
Having mild to moderate depressive symptoms, with or without emotional lability
Experiencing psychological distress

Exclusion Criteria:

Meeting DSM-IV diagnostic criteria for Major Depressive Disorder or another Axis 1 diagnosis
Cognitive impairment
The presence of an unstable medical illness that might preclude completion of the study -

Study is for people with:

Multiple Sclerosis

Phase:

Phase 4

Estimated Enrollment:

20

Study ID:

NCT00151294

Recruitment Status:

Terminated

Sponsor:

Weill Medical College of Cornell University

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There is 1 Location for this study

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NewYork Presbyterian Hospital
White Plains New York, 10605, United States

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Study is for people with:

Multiple Sclerosis

Phase:

Phase 4

Estimated Enrollment:

20

Study ID:

NCT00151294

Recruitment Status:

Terminated

Sponsor:


Weill Medical College of Cornell University

How clear is this clinincal trial information?

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