NCT07350499

Aspiration Thrombectomy Using the Symphony or Prodigy System

Long-Term CLinical Evaluation of Aspiration ThRombectomy Using the Symphony or ProdIgy Thrombectomy System - CLEAR-IT

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 750 (estimated)
• Sponsor: Imperative Care, Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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

• Arterial Thromboembolism
• Venous Thromboembolism
• Pulmonary Embolism

Interventions

Type	Name	Description
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

Timeline

• Start date: 2026-02-13
• Primary completion: 2030-03-01
• Completion: 2030-09-01
• First posted: 2026-01-20
• Last updated: 2026-03-24

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study