New ultrasound method spots low blood flow in spinal cord injuries
NCT ID NCT04056988
First seen Jun 27, 2026 · Last updated Jul 14, 2026 · Updated 2 times
Summary
This study tested whether a special ultrasound with a contrast agent (DEFINITY®) can measure blood flow in the spinal cord during surgery for acute spinal cord injury. 27 patients received the contrast agent while surgeons performed routine decompression. The goal was to see if the technique is feasible and could help doctors detect dangerously low blood flow that may worsen the injury.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Perflutren lipid microsphere (DEFINITY®)
- What this could lead to
- If successful, this technique could help doctors identify low blood flow in the spinal cord and guide treatments to improve outcomes after injury.
- What could go wrong
- This is a small, early feasibility study focused on imaging, not treatment. The technique may not prove useful or may not improve patient recovery.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
27 people
The number who actually took part.
- Started
-
Jul 2018
- Finished
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Nov 2023
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * \>18 * Male or Female * Acute \<72 hours spinal cord injury (ASIA) grade A to D * Medically stable to undergo routine decompression and spinal realignment Exclusion Criteria: * \<18 years of age * Not clinically stable for spinal surgery * Traumatic Brain Injury * Known sensitivity to lipid microsphere or its components i.e., (PEG). * A history of anaphylactoid reactions from ultrasound-enhancing agents
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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
-
Harborview Medical Center
Seattle, Washington, 98104, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Electric jolts to abdominal muscles may restore cough power after spinal injury
- Spinal injury patients may keep stronger bones with simple infusion
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- Spinal zaps could stop dizziness after injury