Safety of Riluzole in Patients With Acute Spinal Cord Injury

NCT00876889 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2017-09-12

No results posted yet for this study

Summary

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).

Conditions

  • Spinal Cord Injury

Interventions

DRUG

Riluzole

50mg PO (by mouth) every 12 hours starting within 12 hours of injury and continuing for 14 days (28 doses).

Sponsors & Collaborators

  • Christopher Reeve Paralysis Foundation

    collaborator OTHER
  • United States Department of Defense

    collaborator FED
  • AO Clinical Investigation and Publishing Documentation

    collaborator OTHER
  • Ontario Neurotrauma Foundation

    collaborator OTHER
  • The Methodist Hospital Research Institute

    lead OTHER

Principal Investigators

  • Robert G Grossman, MD · The Methodist Hospital Research Institute

  • Michael Fehlings, MD, PhD · University of Toronto/Toronto Western Hospital, Toronto

  • Michele M Johnson, MD · the University of Houston/Memorial HermannHospital, Houston

  • Christopher Shaffery, MD · University of Virginia Health System, Charlottesville

  • Susan Harkema, PhD · University of Louisville, Louisville

  • Bizhan Aarabi, MD · University of Maryland Medical Center, Baltimore

  • James Harrop, MD · Thomas Jefferson University, Philadelphia

  • James Guest, MD, PhD · University of Miami, Miami

  • Ralph Frankowski, PhD · The University of Texas School of Public Health, Houston

  • Diana Chow, PhD · University of Houston, College of Pharmacy, Houston

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2011-06-30
Completion
2012-04-30

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00876889 on ClinicalTrials.gov