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IVUS-Guided Treatment for Percutaneous Vascular Interventions

NCT06239493 · Status: SUSPENDED · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2025-05-31

No results posted yet for this study

Summary

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.

Conditions

Interventions

DIAGNOSTIC_TEST

IVUS Guided

Those already undergoing an IVUS guided percutaneous vascular intervention

Sponsors & Collaborators

  • Philips Clinical & Medical Affairs Global

    lead INDUSTRY

Principal Investigators

  • Eric Secemsky, MD · Beth Israel Deaconess Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-14
Primary Completion
2028-02-29
Completion
2028-02-29

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06239493 on ClinicalTrials.gov