IVUS-Guided Treatment for Percutaneous Vascular Interventions

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Conditions studied: CAD, PAD, DVT

In brief

The main objective of the study is to survey and improve the IVUS image quality and X-ray system interoperability by collecting Procedural Data (e.g. raw, pre- processed ultrasound and X-ray data, endpoints such as fluoroscopy time, contrast load and radiation dose, workflow details) during routine intravascular procedures to assure adherence to the high standards of quality during care delivery and promote procedural standardization.

Key facts

Study ID

NCT06239493

Run by

Philips Clinical & Medical Affairs Global

People needed

5000

Starts

2023-09-14

Expected to finish

2028-02-01

Last updated by the study team

2025-05-31

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The Patient is ≥18 years of age.
• Patient is scheduled to undergo percutaneous vascular intervention - peripheral vascular or coronary PCI procedure.

You may not qualify if…

• Patients not meeting the instructions for use (IFU) of the respective IVUS catheters.
• Patients with lesions or vessel segments deemed unsafe for multiple IVUS pullbacks.
• Patients who are pregnant.

Where it is running

• Southwest Cardiovascular Associates — Mesa, Arizona, United States
• Pulse Cardiovascular — Scottsdale, Arizona, United States
• Center for Advanced Cardiac and Vascular Interventions — Tarzana, California, United States
• Pacific Cardiovascular and Vein Institute — Ventura, California, United States
• Community Healthcare System — Munster, Indiana, United States

Full record on ClinicalTrials.gov

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