Multiple Sclerosis Clinical Trial

Escitalopram (Lexapro) for Depression MS or ALS

Summary

The purpose of this study is to see if escitalopram (Lexapro) improves symptoms of major depressive disorder in patients who have ALS or MS.

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Full Description

This eight-week study aims to assess the effectiveness and tolerability of escitalopram in improving symptoms of Major Depression in patients with Amyotrophic Lateral Sclerosis (ALS) or Multiple Sclerosis (MS) as measured by the HAM-D. In addition, the study will assess improvement in the quality of life in patients with Major Depression and ALS or MS.

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Eligibility Criteria

Inclusion Criteria:

Patients between 18 and 70 years of age with documented ALS or MS,
DSM-IV episode of non-psychotic Major Depression,
≥14 score on the 17-item HAM-D,
Ability to give informed consent.

Exclusion Criteria:

History of psychotic disorders,
Psychotic depression,
Bipolar depression,
Suicide risk,
History of substance abuse in the previous 6 months,
History of unstable medical disorders,
Pregnancy or planning for pregnancy,
Severity of ALS or MS that limits participating in the study protocol.

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

13

Study ID:

NCT00965497

Recruitment Status:

Completed

Sponsor:

University of South Carolina

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There is 1 Location for this study

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University of South Carolina School of Medicine
Columbia South Carolina, 20203, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

13

Study ID:

NCT00965497

Recruitment Status:

Completed

Sponsor:


University of South Carolina

How clear is this clinincal trial information?

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