New study aims to sharpen recovery tracking for spinal cord injuries
NCT ID NCT05653206
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 50 adults with incomplete cervical spinal cord injuries to see how well certain tests capture their recovery over 6 months. Researchers will track things like movement, sensation, and balance to find the best ways to measure improvement. The goal is to make future clinical trials more effective by knowing which assessments work best.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2023
- Expected to finish
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Aug 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with traumatic incomplete cervical SCI without instability
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 18-80 years, inclusive * Diagnosis of acute traumatic cervical SCI with ISNCSCI AIS Grade D or sensory deficits only within 92 hours post injury * Cervical neurological level of injury (C2-C8) * MRI, using any imaging protocols (conventional, multiparametric, or quantitative), taken according to standard of care * Presence of spinal cord compression on the MRI * Absence of biomechanical instability to the extent that would mandate stabilization surgery by the treating surgeon * Ability to provide informed consent according to the IRB/EC defined and approved procedures Exclusion Criteria: * Nontraumatic SCI * Concomitant traumatic brain injury or polytrauma that could preclude accurate or reliable assessments of the outcome assessments * Uncontrolled severe systemic diseases, preexisting neurological, musculoskeletal, or general medical conditions which could preclude accurate assessments or FUs * Individuals unable to undergo MRI
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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BG Klinikum Murnau gGmb, BGU Murnau, Trauma Center Murnau
Murnau am Staffelsee, 82418, Germany
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Indian Spinal Injuries Centre
New Delhi, 110070, India
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Instituto de Ortopedia E Traumatologia Do Hospital Das Clinicas Da Universidade de Sao Paulo
São Paulo, 05403-010, Brazil
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Medical college of Winsconsine, Neurosurgery
Milwaukee, Wisconsin, 53226, United States
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Orthopaedics, Centro Hospitalar Universitário do Porto
Porto, 4099-001, Portugal
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San Francisco General Hospital
San Francisco, California, 94143, United States
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St. Michael's Hospital
Toronto, M5B1W8, Canada
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Toronto Western Hospital University Health Network
Toronto, M6S2W5, Canada
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UMD STC Neurosurgery Clinic
Baltimore, Maryland, 21201, United States
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Vancouver Spine Research Program, Blusson Spinal Cord Centre
Vancouver, V5Z 1M9, Canada
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