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Aspiration Thrombectomy Using the Symphony or Prodigy System

NCT07350499 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2026-05-18

No results posted yet for this study

Summary

The study is designed to evaluate the short-term and long-term clinical performance and safety of the Symphony and Prodigy thrombectomy systems used in endovascular procedures across the peripheral or pulmonary vasculature.

Conditions

Interventions

DEVICE

Prodigy Thrombectomy System

Removal of thrombus/emboli from blood vessels in the peripheral vasculature

DEVICE

Symphony Thrombectomy System

Removal of thrombus/emboli from blood vessels in the peripheral vasculature

DEVICE

Symphony Thrombectomy System

Removal of thrombus/emboli from the pulmonary vasculature

Sponsors & Collaborators

  • Imperative Care, Inc.

    lead INDUSTRY

Principal Investigators

  • Steven Abramowitz, MD · Medstar Health Research Institute

  • Maya Serhal, MD · Massachusetts General Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-13
Primary Completion
2030-03-31
Completion
2030-09-30
FDA Device
Yes

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 NCT07350499 on ClinicalTrials.gov