Spinal Cord Injury Registry - North American Clinical Trials Network
Recruiting
Observational Study
Spinal Cord Injury
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
1,500 (estimated)
Sponsor
Robert G. Grossman, MD · Other
Who this trial is looking for
This trial is looking for adults who have had a first-time spinal cord injury due to trauma. Participants will share information about their injury and treatment over the first year to help understand spinal cord injuries better.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I have a first-time spinal cord injury caused by trauma.
I have paralysis or loss of sensation.
I have not received prior treatment for this injury.
I agree to give my consent to participate.
You may not be able to join if
I or my family do not want to give consent.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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 m…
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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).
* Has not received prior medical of surgical care for this injury at an intermedia…
Inclusion Criteria:
* 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).
* Has not received prior medical of surgical care for this injury at an intermediate hospital.
* Must give informed consent
Exclusion Criteria:
* Any patient or family refusing consent
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