Safety of Riluzole in Patients With Acute Spinal Cord Injury



Status:Completed
Conditions:Hospital, Orthopedic
Therapuetic Areas:Orthopedics / Podiatry, Other
Healthy:No
Age Range:18 - 70
Updated:9/13/2017
Start Date:April 2010
End Date:April 2012

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Safety and Pharmacokinetics of Riluzole in Patients With Traumatic Acute Spinal Cord Injury

The purpose of the study is to find out if the use of the drug Riluzole is both safe and
improves outcome in patients with acute traumatic spinal cord injury (SCI).

The primary aim of the study is to develop acute care safety and pharmacokinetic profiles of
riluzole in patients who have sustained a acute traumatic spinal cord injury. Secondary
objectives are to conduct exploratory analyses of functional outcomes for purposes of
planning a subsequent Phase II randomized study of the efficiency of Riluzole for the
treatment of acute traumatic spinal cord injury.

Inclusion Criteria:

- Age equal to or greater than 18 years and less than or equal to 70 years;

- Willing to give written informed consent to participate in the study. The informed
consent may require legally authorized representative to sign if arm/hand function is
compromised.

- No other life-threatening injury

- Spinal cord injury at the neurologic level from C4 to T12

- ASIA Impairment Scale level A, B or C

- No cognitive impairment which would preclude an informed consent (including moderate
or severe traumatic brain injury)

- Less than 12 hours since injury

Exclusion Criteria:

- Equal or more than 12 hours since injury

- Hypersensitivity to riluzole or any of its components

- Unable to receive riluzole orally or via nasogastric tube

- History of liver or kidney disease (e.g. Hepatitis A, B or C, Cirrhosis, etc.)

- Has a recent history of regular substance abuse (illicit drugs, alcohol)

- Unconscious

- Penetrating spinal cord injury

- Pregnancy as established by urine pregnancy test

- Breastfeeding

- Life expectancy less than 12 months

- Is currently involved in another therapeutic SCI research study that precludes or
complicates participation in this study (e.g. study of another therapeutic drug aiming
for spinal cord injury recovery, any study that substantially interferes with the
follow -up schedule (f/u) schedule, or any high risk study that complicates evaluation
of safety outcomes. Types of studies that would not preclude participation are e.g.
behavioral adaptation studies, mental health interventions)

- Has a mental disorder or other illness, which in the view of the site investigator,
would preclude accurate evaluation (e.g. schizophrenia, severe cognitive disability,
Parkinson disease)

- Unable to commit to the follow-up schedule

- Is a prisoner

- Unable to converse, read or write English at the elementary school level
We found this trial at
8
sites
Houston, Texas 77030
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Miami, Florida 33124
(305) 284-2211
University of Miami A private research university with more than 15,000 students from around the...
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Miami, FL
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22 S Greene St
Baltimore, Maryland 21201
(410) 328-8667
University of Maryland Medical Center Founded in 1823 as the Baltimore Infirmary, the University of...
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Baltimore, MD
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1215 Lee St
Charlottesville, Virginia 22903
(434) 924-0211
University of Virginia Health System UVA Health System includes a 604-bed hospital, level I trauma...
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Charlottesville, VA
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Houston, Texas 77030
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Houston, TX
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Louisville, KY
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1020 Walnut St
Philadelphia, Pennsylvania 19107
(215) 955-6000
Thomas Jefferson University We are dedicated to the health sciences and committed to educating professionals,...
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Philadelphia, PA
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Toronto,
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