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NCT06654804 · ClinicalTrials.gov registry record · Phase 4
Contrast-enhanced Ultrasound in the Treatment of Acute Spinal Cord Injury
A Phase 4 study of Acute Spinal Cord Injury, sponsored by University of Washington.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT06654804 is a Phase 4 study of Acute Spinal Cord Injury that is actively recruiting participants, run by University of Washington. The registered enrollment target is 50 participants, above the 35-participant average among 8 other Acute Spinal Cord Injury trials with a reported enrollment target (43% higher). The trial reports 1 study location across 1 state.
The verdict
NCT06654804, a Phase 4 study of Acute Spinal Cord Injury, is actively recruiting participants, sponsored by University of Washington.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
Patients with traumatic spinal cord injury (tSCI) often suffer from spinal cord swelling inside the thecal sac, which contains the spinal cord and surrounding fluid, leading to increased pressure on the spinal cord tissue and decreased spinal cord blood flow at the site of injury. The combination of increased pressure and decreased blood flow causes vascular hypoperfusion of the spinal cord and exacerbates the severity of injury. This is also referred to as secondary injury. Thus, knowledge of spinal cord hypoperfusion would allow the treating physician to optimize the hemodynamic condition of the patient with acute spinal cord injury and potentially improve functional outcomes.
Conditions Studied
Interventions
- DRUG Perflutren lipid
Study Locations (1)
Washington
- University of Washington Harborview Medical Center - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2023-09-28 |
| Est. Completion | 2027-09-15 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06654804
The ClinicalTrials.gov registry entry for NCT06654804 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 35-participant average among 8 other Acute Spinal Cord Injury trials with a reported enrollment target (43% higher). The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Acute Spinal Cord Injury appearing as the primary indexed condition, and to 1 intervention - of which Perflutren lipid is the first listed.
NCT06654804 reports 1 study location spanning 1 distinct geographic area - top geographies include Washington.
Frequently Asked Questions
What is clinical trial NCT06654804 about?
NCT06654804 is a clinical study titled "Contrast-enhanced Ultrasound in the Treatment of Acute Spinal Cord Injury". Patients with traumatic spinal cord injury (tSCI) often suffer from spinal cord swelling inside the thecal sac, which contains the spinal cord and surrounding fluid, leading to increased pressure on the spinal cord tissue and decreased spinal cord blood flow at the site of injury. The combination of...
What is the current status of trial NCT06654804?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 50 participants. The study started on 2023-09-28. Estimated completion is 2027-09-15.
What conditions does trial NCT06654804 study?
This clinical trial studies the following conditions: Acute Spinal Cord Injury.
What interventions are being tested in trial NCT06654804?
The interventions under investigation include: Perflutren lipid (DRUG).
Who is sponsoring clinical trial NCT06654804?
This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06654804 being conducted?
This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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