CEUS For Intraoperative Spinal Cord Injury

NACompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

December 1, 2023

Primary Completion Date

August 1, 2025

Study Completion Date

August 1, 2025

Conditions
Spine DiseaseSpinal StenosisSpinal InjurySpinal Cord DiseasesSpinal Cord InjuriesSpinal Cord CompressionSpine Degeneration
Interventions
DEVICE

Definity Perflutren Lipid Microsphere Ultrasound Contrast

"1. Before the spinal decompression surgery has started, the study team will inject the ultrasound contrast to visualize the spinal cord prior to decompression of the spinal cord.~2. After the spinal cord has been decompressed, the study team will inject the ultrasound contrast to visualize the spinal cord directly after decompression of the spinal cord.~3. Prior to completion and closure of the incision, the study team will once more inject the ultrasound contrast to visualize the spinal cord.~4. A member of the research team will follow up with study participants within a week of the procedure by phone. The research staff will also review the participants' medical record for up to 360 days after your procedure to collect information on clinical outcomes and any additional treatments, tests or procedures the study participants may have had."

Trial Locations (1)

29425

Medical University of South Carolina, Charleston

All Listed Sponsors
collaborator

South Carolina Spinal Cord Injury Research Fund

UNKNOWN

lead

Medical University of South Carolina

OTHER

NCT05530798 - CEUS For Intraoperative Spinal Cord Injury | Biotech Hunter | Biotech Hunter