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| Sponsors and Collaborators: |
National Institute of Neurological Disorders and Stroke (NINDS) Massachusetts General Hospital |
| Information provided by: | Office of Rare Diseases (ORD) |
| ClinicalTrials.gov Identifier: | NCT00004457 |
Purpose
OBJECTIVES:
I. Determine specific clinical features, molecular abnormalities, and laboratory-based biological markers of free radical stress that are associated with amyotrophic lateral sclerosis and influence disease severity.
| Condition |
|
Amyotrophic Lateral Sclerosis |
| Genetics Home Reference related topics: | amyotrophic lateral sclerosis |
| MedlinePlus related topics: | Amyotrophic Lateral Sclerosis |
| Study Type: | Observational |
| Study Design: | Screening, Defined Population, Prospective Study |
| Estimated Enrollment: | 75 |
| Study Start Date: | March 1998 |
PROTOCOL OUTLINE: This is a screening and diagnostic study. Blood and urine samples are collected from patients every 2 months for 1 year. All samples are evaluated for measures of free radical damage and levels of the body's own antioxidant activity.
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics-- Clinically diagnosed probable or definite, sporadic or familial amyotrophic lateral sclerosis
--Patient Characteristics-- Pulmonary: No artificial ventilation required Other: No other neurodegenerative diseases No concurrent or history of unstable medical illness
Contacts and Locations| National Institute of Neurological Disorders and Stroke (NINDS) |
| Massachusetts General Hospital |
| Study Chair: | Merit E. Cudkowicz | Massachusetts General Hospital |
More Information
| Study ID Numbers: | 199/13650, MGH-97-7231, MGH-1K08NS01896 |
| First Received: | October 18, 1999 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00004457 |
| Health Authority: | United States: Federal Government |
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