Aspiration Thrombectomy Using the Symphony or Prodigy System

Part of paid clinical trials in Huntsville, Alabama.

Sponsor
Imperative Care, Inc.
Study ID
NCT07350499
Status
Recruiting

Conditions

  • Arterial Thromboembolism
  • Pulmonary Embolism
  • Venous Thromboembolism

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Prodigy Thrombectomy System — DEVICE
    Removal of thrombus/emboli from blood vessels in the peripheral vasculature
  • Symphony Thrombectomy System — DEVICE
    Removal of thrombus/emboli from blood vessels in the peripheral vasculature
  • Symphony Thrombectomy System — DEVICE
    Removal of thrombus/emboli from the pulmonary vasculature

Study Details

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.

Key Dates

Start date
Feb 13, 2026
Status verified
Feb 2026
Primary completion
Mar 31, 2030
Completion
Sep 30, 2030

Study Design

Enrollment
750 participants (estimated)

Arms

  • Arm: Peripheral Arterial
    Subjects in this cohort will undergo aspiration thrombectomy to remove thrombus from the peripheral arterial vasculature
  • Arm: Peripheral Venous
    Subjects in this cohort will undergo aspiration thrombectomy to remove thrombus from the peripheral venous vasculature
  • Arm: Pulmonary Embolism
    Subjects in this cohort will undergo aspiration thrombectomy to remove thrombus from the pulmonary vasculature

Primary Outcome Measure

Peripheral Arterial Cohort [ Time Frame: 30 days ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Huntsville HospitalHuntsvilleAlabama35801-
Profound ResearchMunsterIllinois46321-

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