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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00922831
Other study ID # 080514
Secondary ID
Status Withdrawn
Phase
First received June 16, 2009
Last updated April 10, 2018
Start date August 2008
Est. completion date August 2013

Study information

Verified date April 2018
Source MidAmerica Neuroscience Research Foundation at Rowe Neurology Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to look at multiple sclerosis patients process of awareness, learning, and judging status over a 3 year time period.


Description:

Patients with multiple sclerosis (MS) frequently experience cognitive and emotional difficulties. Theses neuropsychiatric symptoms are known to be associated with reduced quality of life. However, little is known about the evolution of MS patients' neuropsychiatric difficulties and how these neuropsychiatric changes may be related to other MS symptoms. The purpose of the present study is to examine MS patients' cognitive and emotional status over time as part of standard neuropsychological evaluations in a private practice setting. MS patients presenting for neuropsychological evaluation at the MidAmerica Neuroscience Institute will be provided with the option of participating in thorough evaluation of their cognitive and affective MS symptoms. They will then be followed clinically and receive re-evaluation over a period of 3 years on a yearly basis. It is hoped that this study will help us obtain a better understanding of the factors associated with worsening cognition in MS. A greater understanding of the factors associated with cognitive and affective decline in MS help could lead to the early identification and treatment of at-risk patients.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date August 2013
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Male/female subjects at least 18 years of age with a diagnosis of Clinically Definite Multiple Sclerosis (CDMS) or Clinically Isolated Syndrome (CIS)as confirmed by a neurologist.

- Subjects must be able to give written informed consent and comply with the study protocol. Subjects must also be able to read, write and understand English.

- Are capable of performing the requirements of the neuropsychological test battery.

Exclusion Criteria:

- As judged by the investigator, any clinically significant, unstable or major concomitant disorder or medications.

- In the opinion of the Investigator should not participate in the study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
MidAmerica Neuroscience Research Foundation at Rowe Neurology Institute University of Missouri, Kansas City
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