RECRUITING

Spinal Cord Injury Registry - North American Clinical Trials Network

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Spinal Cord Injury Registry - North American Clinical Trials Network for Spinal Cord Injury

Quick Facts

Study Start:2005-07
Study Completion:2028-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT00178724

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Any patient male or female \> or equal to 18 years of age with first time spinal cord injury caused by trauma and has neurological deficit with paralysis (weakness) or loss of sensation (touch).
  2. * Has not received prior medical of surgical care for this injury at an intermediate hospital.
  3. * Must give informed consent
  1. * Any patient or family refusing consent

Contacts and Locations

Study Contact

Elizabeth G Toups, MSN, RN, CCRP
CONTACT
832-722-4055
etoups@houstonmethodist.org
Tanisha Bernhardt
CONTACT
713-441-3814

Principal Investigator

Robert G Grossman, MD
STUDY_CHAIR
Houston Methodist Hospital, Houston
Karl M Schmitt, MD
PRINCIPAL_INVESTIGATOR
The University of Texas, Houston
Michael G Fehlings, MD, PhD
PRINCIPAL_INVESTIGATOR
University of Toronto/Toronto Western Hospital, Toronto
Emily Sieg, MD
PRINCIPAL_INVESTIGATOR
University of Louisville, Louisville
Bizhan Aarabi, MD
PRINCIPAL_INVESTIGATOR
University of Maryland Medical Center, Baltimore Shock Trauma Center
Chun-Po Yen, MD
PRINCIPAL_INVESTIGATOR
University of Virginia Health System, Charlottesville
Christopher J Neal, MD
PRINCIPAL_INVESTIGATOR
Walter Reed National Military Medical Center, Bethesda
James S Harrop, MD
PRINCIPAL_INVESTIGATOR
Thomas Jefferson University, Philadelphia
James D Guest, MD, PhD
PRINCIPAL_INVESTIGATOR
University of Miami, Miami
Ryan P Morton, MD
PRINCIPAL_INVESTIGATOR
Brooke Army Medical Center, Fort Sam Houston
Jason D Wilson, MD
PRINCIPAL_INVESTIGATOR
Louisiana State University Health Sciences Center in New Orleans
Hamid Shah, MD
PRINCIPAL_INVESTIGATOR
Vanderbilt University Medical Center, Nashville
Shekar N Kurpad, MD, PhD
PRINCIPAL_INVESTIGATOR
Medical College of Wisconsin, Milwaukee
Christopher I Shaffrey, MD
PRINCIPAL_INVESTIGATOR
Duke University, Durham

Study Locations (Sites)

University of Miami
Miami, Florida, 33136
United States
University of Louisville Health Sciences Center
Louisville, Kentucky, 40205
United States
Louisiana State University Medical Sciences Center in New Orleans
New Orleans, Louisiana, 70112
United States
University of Maryland Medical Center
Baltimore, Maryland, 21201
United States
Walter Reed National Military Medical Center
Bethesda, Maryland, 20889
United States
Duke University
Durham, North Carolina, 27710
United States
Thomas Jefferson University
Philadelphia, Pennsylvania, 19107
United States
Hamid Shah, MD
Nashville, Tennessee, 37240
United States
Brooke Army Medical Center
Fort Sam Houston, Texas, 78234
United States
Houston Methodist Hospital
Houston, Texas, 77030
United States
The University of Texas, Houston
Houston, Texas, 77030
United States
University of Virginia Health System
Charlottesville, Virginia, 22903
United States
Medical College of Wisconsin
Milwaukee, Wisconsin, 53226
United States

Collaborators and Investigators

Sponsor: Robert G. Grossman, MD

  • Robert G Grossman, MD, STUDY_CHAIR, Houston Methodist Hospital, Houston
  • Karl M Schmitt, MD, PRINCIPAL_INVESTIGATOR, The University of Texas, Houston
  • Michael G Fehlings, MD, PhD, PRINCIPAL_INVESTIGATOR, University of Toronto/Toronto Western Hospital, Toronto
  • Emily Sieg, MD, PRINCIPAL_INVESTIGATOR, University of Louisville, Louisville
  • Bizhan Aarabi, MD, PRINCIPAL_INVESTIGATOR, University of Maryland Medical Center, Baltimore Shock Trauma Center
  • Chun-Po Yen, MD, PRINCIPAL_INVESTIGATOR, University of Virginia Health System, Charlottesville
  • Christopher J Neal, MD, PRINCIPAL_INVESTIGATOR, Walter Reed National Military Medical Center, Bethesda
  • James S Harrop, MD, PRINCIPAL_INVESTIGATOR, Thomas Jefferson University, Philadelphia
  • James D Guest, MD, PhD, PRINCIPAL_INVESTIGATOR, University of Miami, Miami
  • Ryan P Morton, MD, PRINCIPAL_INVESTIGATOR, Brooke Army Medical Center, Fort Sam Houston
  • Jason D Wilson, MD, PRINCIPAL_INVESTIGATOR, Louisiana State University Health Sciences Center in New Orleans
  • Hamid Shah, MD, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center, Nashville
  • Shekar N Kurpad, MD, PhD, PRINCIPAL_INVESTIGATOR, Medical College of Wisconsin, Milwaukee
  • Christopher I Shaffrey, MD, PRINCIPAL_INVESTIGATOR, Duke University, Durham

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2005-07
Study Completion Date2028-07

Study Record Updates

Study Start Date2005-07
Study Completion Date2028-07

Terms related to this study

Keywords Provided by Researchers

  • spinal cord injury
  • SCI
  • traumatic spinal cord injury
  • acute spinal cord injury
  • paralysis

Additional Relevant MeSH Terms

  • Spinal Cord Injury