Non-invasive Flow Measurements in Patients With Lower Extremity Arterial Disease (LEAD)

Philips

Status: Enrolling

Conditions: Lower Extremity Arterial Disease

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT05689190

ICBE-S-000115

Details and patient eligibility

About

This concerns a study with patients who will undergo endovascular treatment. Blood flow will be measured by 2D Duplex Ultrasound. Contrast data will be collected that will be processed offline.

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients referred to the vascular surgery outpatient clinic (LUMC) with PAD
• Age ≥18 years
• Superficial femoral artery (SFA) stenosis (>70% occluded)
• Elective for a percutaneous transluminal angioplasty procedure
• Written informed consent

Exclusion criteria

• Contraindications to angiography, such as severe renal insufficiency (eGFR< 20)
• Non-correctable bleeding disorder.

Trial design

30 participants in 1 patient group

patients

Description:

Duplex ultrasound, angiogram, PTA intervention