Spinal Cord Injury Registry - North American Clinical Trials Network

NCT00178724 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2020-09-24

No results posted yet for this study

Summary

The NACTN Spinal Cord Injury Registry is a network of clinical centers collecting de-identified data from patients admitted through the Emergency Department of a NACTN center at the time of injury with an initial (first time) spinal cord injury (SCI). Information will be collected on the natural history of SCI and course of treatment through the first 12 months from the date of injury or long as medically indicated. Data collected includes imaging information from CT or MRI scans, neurological and general medical outcome and rehabilitation evaluation. No intervention is given other than standard of care for spinal cord injury, intensive monitoring and frequent follow up care.

Conditions

  • Spinal Cord Injury

Interventions

OTHER

No Treatment Given

Intervention is not given.

Sponsors & Collaborators

  • Christopher Reeve Paralysis Foundation

    collaborator OTHER
  • The Methodist Hospital Research Institute

    collaborator OTHER
  • The University of Texas Health Science Center, Houston

    collaborator OTHER
  • University of Virginia

    collaborator OTHER
  • University of Louisville

    collaborator OTHER
  • University of Toronto

    collaborator OTHER
  • University of Maryland, Baltimore

    collaborator OTHER
  • Walter Reed National Military Medical Center

    collaborator FED
  • Thomas Jefferson University

    collaborator OTHER
  • University of Miami

    collaborator OTHER
  • Brooke Army Medical Center

    collaborator FED
  • Louisiana State University Health Sciences Center in New Orleans

    collaborator OTHER
  • Vanderbilt University Medical Center

    collaborator OTHER
  • Medical College of Wisconsin

    collaborator OTHER
  • Duke University

    collaborator OTHER
  • Robert G. Grossman, MD

    lead OTHER

Principal Investigators

  • Robert G Grossman, MD · Houston Methodist Hospital, Houston

  • Karl M Schmitt, MD · The University of Texas, Houston

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

  • Emily Sieg, MD · University of Louisville, Louisville

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

  • Chun-Po Yen, MD · University of Virginia Health System, Charlottesville

  • Christopher J Neal, MD · Walter Reed National Military Medical Center, Bethesda

  • James S Harrop, MD · Thomas Jefferson University, Philadelphia

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

  • Ryan P Morton, MD · Brooke Army Medical Center, Fort Sam Houston

  • Jason D Wilson, MD · Louisiana State University Health Sciences Center in New Orleans

  • Hamid Shah, MD · Vanderbilt University Medical Center, Nashville

  • Shekar N Kurpad, MD, PhD · Medical College of Wisconsin, Milwaukee

  • Christopher I Shaffrey, MD · Duke University, Durham

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-07-31
Primary Completion
2025-07-31
Completion
2028-07-31

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 NCT00178724 on ClinicalTrials.gov