Phase
Condition
Spinal Cord Injuries
Spinal Stenosis
Spinal Cord Disorders
Treatment
Definity Perflutren Lipid Microsphere Ultrasound Contrast
Clinical Study ID
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients consented and scheduled for posterior cervicothoracic decompression surgerywith the PI for the diagnosis of cervicothoracic myeloradiculopathy
Age 18-80
Exclusion
Exclusion Criteria:
Pregnancy
Patient's with known hypersensitivity to ultrasound contrast
Patients with known hypersensitivity to perflutren lipid microsphere or itscomponents, such as polyethylene glycol (PEG)
Patients unable to actively participate in the consent process physically and/orcognitively
Prior decompression at the intended level of decompression
Study Design
Connect with a study center
Medical University of South Carolina
Charleston, South Carolina 29425
United StatesSite Not Available
Medical University of South Carolina
Charleston 4574324, South Carolina 4597040 29425
United StatesSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.