๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2020-09-22

Spinal Cord Injury Registry - North American Clinical Trials Network (NCT00178724)

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

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: Robert G. Grossman, MD

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: University of Miami โ€” Miami, Florida

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • No Treatment Given (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (14 Sites)

  • University of Miami โ€” Miami, Florida
  • University of Louisville Health Sciences Center โ€” Louisville, Kentucky
  • Louisiana State University Medical Sciences Center in New Orleans โ€” New Orleans, Louisiana
  • University of Maryland Medical Center โ€” Baltimore, Maryland
  • Walter Reed National Military Medical Center โ€” Bethesda, Maryland
  • Duke University โ€” Durham, North Carolina
  • Thomas Jefferson University โ€” Philadelphia, Pennsylvania
  • Hamid Shah, MD โ€” Nashville, Tennessee
  • Brooke Army Medical Center โ€” Fort Sam Houston, Texas
  • Houston Methodist Hospital โ€” Houston, Texas
  • The University of Texas, Houston โ€” Houston, Texas
  • University of Virginia Health System โ€” Charlottesville, Virginia
  • Medical College of Wisconsin โ€” Milwaukee, Wisconsin
  • University of Toronto/Toronto Western Hospital โ€” Toronto, Ontario

๐Ÿ“ž Contact the Study Coordinator

Phone: (832) 722-4055

Email: etoups@houstonmethodist.org

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—