Expired Study
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Charlottesville, Virginia 22908


Purpose:

R(+)pramipexole is administered in escalating doses to patients with early ALS. Plasma and spinal fluid levels of R(+)PPX are monitored, in addition to biochemical markers of oxidative stress.


Criteria:

Inclusion Criteria: - definite ALS no prior exposure to R(+)PPX Exclusion Criteria: - ALSFRS at baseline <40 FVC at baseline <70%


NCT ID:

NCT00600873


Primary Contact:

Principal Investigator
Ted M Burns, MD
University of Virginia


Backup Contact:

N/A


Location Contact:

Charlottesville, Virginia 22908
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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