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Case-Specific Health Care Professional Clinical Survey of Liberant™ Thrombectomy System

Key facts

Who runs it
Medtronic Endovascular
Where
Brooklyn, Naples, New York, Plano, Scottsdale, and Washington D.C., United StatesSee the 6 sites
Trial code
Status
Completed
People taking part
51 people enrolled
Started
24 Feb 2026
Ended
30 Oct 2026
Type of study
Observational
Treatments tested
  • Liberant Thrombectomy System
Record updated
6 November 2026

Who can take part

Age
22 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 3 criteriaShow less

Other criteria

  • Patient case selection to be included in the clinical assessment will be specific to Liberant and will be made according to the following criteria:
  • Patient treated is age ≥ 22 years at the time of procedure
  • Use of Liberant in accordance with the device labeling within 72 hours of index procedure

Where in United States

  • NewYork-Presbyterian Medical Group BrooklynBrooklyn, United StatesNo longer taking part
  • Naples Comprehensive HealthNaples, United StatesNo longer taking part
  • Mount SinaiNew York, United StatesNo longer taking part
  • Baylor Heart Hospital Of PlanoPlano, United StatesNo longer taking part
  • HonorHealth Heart Care - Vascular - OsbornScottsdale, United StatesNo longer taking part
  • MedStar HealthWashington D.C., United StatesNo longer taking part

About the trial

What the trial wants to find out

The purpose of Case-Specific Health Care Professional (HCP) Clinical Survey of Liberant™ Thrombectomy System, also known as the Liberant Clinical Assessment, is to collect first-in-human clinical data to confirm the safety and performance of the Medtronic Liberant™ thrombectomy system when used for the removal of fresh, soft emboli or thrombi from the vessels of the peripheral arterial and venous systems

Treatments tested

  • Liberant Thrombectomy System

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Record updated
6 November 2026