Long-Term CLinical Evaluation of Aspiration ThRombectomy Using the Symphony or ProdIgy Thrombectomy System - CLEAR-IT
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Subject is ≥ 18 years of age
• Subject is willing and able to comply with the follow-up schedule specified in this protocol
• Subject is willing and able to provide written informed consent prior to any study-related data collection
• Subject has a planned procedure, involving the use of Imperative Care vascular devices within their intended use
Locations
United States
Alabama
Huntsville Hospital
RECRUITING
Huntsville
Contact Information
Primary
Sylvie Akiel-Fu, MPH
safu@imperativecare.com
917-375-4735
Time Frame
Start Date: 2026-02-13
Estimated Completion Date: 2030-09
Participants
Target number of participants: 750
Treatments
Peripheral Arterial
Subjects in this cohort will undergo aspiration thrombectomy to remove thrombus from the peripheral arterial vasculature
Peripheral Venous
Subjects in this cohort will undergo aspiration thrombectomy to remove thrombus from the peripheral venous vasculature
Pulmonary Embolism
Subjects in this cohort will undergo aspiration thrombectomy to remove thrombus from the pulmonary vasculature
Related Therapeutic Areas
Sponsors
Leads: Imperative Care, Inc.