North American Clinical Trials Network (NACTN) for Treatment of Spinal Cord Injury - NCT00178724-40205 (Clinical Trial 129087)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy129087.aspx
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| City: |
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Louisville |
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State:
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KY |
| Zip Code: |
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40205 |
| Conditions: |
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Spinal Cord Injury |
| Purpose: |
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The NACTN Registry is a network of clinical centers collecting standardized de-identified
data from patients presenting with a new traumatic spinal cord injury(SCI). Information
will be collected on the natural history of SCI and course of treatment through the first 12
months following the date of injury. Data collected includes imaging information from CT or
MRI scans, neurological and general medical outcome and rehabilitation evaluation.
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| Study summary: |
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The participating centers include:
The Methodist Hospital, Houston; Northwestern University-Rehabilitation Institute of
Chicago; University of Texas Health Science Center, Houston; University of Toronto, Toronto;
University of Virginia, Charlottesville; University of Louisville, Louisville; University of
Maryland, Baltimore
The Biostatistics and Data Management Center is at:
The University of Texas School of Public Health, Houston.
Preliminary work has been completed on the selection of data elements, data collection
protocols, case record form design, and the design of a computer system for clinical data
management and data quality control.
In the first phase of the network, data will be collected on the natural history of SCI.
Although there is considerable data in the literature about the natural history of SCI,
current changes in treatment appear to be modifying the natural history. In particular very
early surgery, including decompression of the spinal cord and vertebral stabilization with
instrumentation appears, in some cases of SCI, to be improving outcomes. |
| Criteria: |
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Inclusion Criteria:
- Any patient male or female > or equal to 18 years of age with an initial traumatic
spinal cord injury adn neurological deficit ( motor weakness/paralysis or loss of
sensation).
- Must give informed consent
Exclusion Criteria:
- Any patient/family refusing consent |
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| Study is available at: |
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University of Louisville Health Sciences Center
Louisville, KY 40205
United States
Primary Contact:
Elizabeth Toups, MS, RN
Email: etoups@tmhs.org
Phone: 713-441-3897 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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February 15, 2010 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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