The objective of the clinical trial is to gather evidence on the safety, performance and clinical efficacy Vibrato Sleeve TUS in people with peripheral artery disease (PAD).
Subjects will be randomized to a test or control group and will receive an active or sham Vibrato Sleeve respectively. Those randomized to the control arm will undergo therapy sessions with a sham Vibrato Sleeve device and two months of follow-up. Upon completion of the 2-month follow-up visit, subjects will be informed of their randomization assignment. Subjects in the sham arm will be allowed to crossover to a treatment regimen that uses an active Vibrato Sleeve device and will follow the same visit schedule as the active test group.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
29
This device delivers ultrasound energy to the targeted area of the lower limb.
Vascular & Interventional Specialists of Orange County
Orange, California, United States
Changes in foot perfusion
Mean difference between pre-treatment (baseline) and/or last sham treatment with post-treatment measurements, including the 2-month follow-up.
Time frame: 4 months
Adverse Events
Analysis of all reported device-related adverse events throughout each subject's participation.
Time frame: up to and including the 2-month follow-up visit for test and control subjects.
Subject Questionnaire
Questions will be based on each treatment session and what each subject felt and observed.
Time frame: up to and including the 2-month follow-up visit for test and control subjects.
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