Minimally Invasive Treatment of Primary Great Saphenous Vein (GSV) Insufficiency Using High Intensity Focused Ultrasound (HIFU)
Completed · Not applicable
Conditions studied: Great Saphenous Vein Insufficiency
In brief
This is a one-arm, open label, prospective, single-center study. Primary objective To evaluate the feasibility of HIFU for treatment of Great Saphenous Vein using assessments of patient experience and response to treatment. Secondary objective To assess the general safety and ablation rate outcomes following HIFU treatment of GSV
Key facts
- Study ID
- NCT05193643
- Run by
- Englewood Hospital and Medical Center
- People needed
- 20
- Starts
- 2022-03-23
- Expected to finish
- 2023-01-31
- Last updated by the study team
- 2023-04-19
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Candidate for venous procedure with primary GSV insufficiency involving reflux in the segment to be treated
- CEAP-clinical classification ≥ 2
- Physical condition allowing ambulation after the procedure.
- Agree to comply with the Clinical investigation plan and follow-up schedule of the study
- Targeted tissue reachable for treatment with the device - meaning between 5mm and 24mm below the skin surface.
- Age over 22 years at the time of enrollment.
- No acute venous thrombosis.
- No complete or near complete deep vein post-thrombotic disease.
- Patient has signed and understood the written informed consent.
You may not qualify if…
- Patient is pregnant
- Known allergic reaction to anesthetics to be used.
- Legally incapacitated or imprisoned patients
- Patient's vein target not clearly visible on the ultrasound images (in B mode) at the inclusion visit.
- Patient participating in another clinical trial involving an investigational drug or device.
- Ankle-brachial index <7 (ABI)
- Undergoing active anticoagulant therapy within the last 6 months
- Diameter of the treated anatomical segment below ≤ 2mm
Where it is running
- Englewood Health — Englewood, New Jersey, United States
Full record on ClinicalTrials.gov
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