Could your own growth factors help heal a spinal cord injury?
NCT ID NCT07253233
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase study tests whether a concentrated form of the patient's own growth factors can improve motor function after a spinal cord injury. Ten adults with moderate to severe traumatic spinal cord injury will receive the treatment. The goal is to see if this approach can restore some movement and offer a new option for managing this devastating condition.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Jul 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.
- Ages
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18 to 60 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Chinese citizens, aged 18-60; * Spinal cord injury caused by trauma; * ASIA spinal cord injury grade C-D; ④ Duration of the disease: Acute, subacute and chronic spinal cord injuries are all acceptable; ⑤ Cooperate to complete the follow-up. Exclusion Criteria: * Severe systemic diseases; * Joint contractures; * Having hematological diseases, autoimmune diseases and infectious diseases; * Prohibited conditions for magnetic resonance imaging and electrophysiological examinations(For example:intracranial metal implants, cardiac stents, spinal stimulators, spinal internal fixators); * Severe anxiety/depression/manic states, or diagnosed with mental illness or epilepsy; ⑥ Spinal cord injury caused by myelitis, multiple sclerosis, or spinal tumors; * Complicated with bleeding disorders or coagulation dysfunction; * Individuals with osteoporosis and a high risk of pathological fractures; ⑨ Poor compliance, or unable to correctly understand and cooperate to complete follow-up; ⑩ Pregnant or lactating women; ⑪ Those who have received other spinal cord injury intervention treatments such as stem cells or growth factors within the past 3 months.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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