Tundra Space

Tundra Space

Book DemoDirectoryLog InSign Up

Clinical Research Directory

Browse clinical research sites, groups, and studies.

SitesGroupsStudies
Back to Studies
NOT YET RECRUITING
NCT07335341

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

Sponsor: Medtronic Endovascular

View on ClinicalTrials.gov

Summary

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

Key Details

Gender

All

Age Range

22 Years - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2026-03

Completion Date

2026-08

Last Updated

2026-03-04

Healthy Volunteers

No

Conditions

Venous Embolism of Lower Extremities (Diagnosis)Arterial Embolism and ThrombosisAcute DVT of Lower ExtremityChronic DVT of Lower ExtremityDVTDeep Vein Thrombosis LegThrombus in the Peripheral Venous VasculaturePeripheral Arterial DiseaseAcute Limb IschemiaLower Extremity Acute Limb IschemiaLE ALI

Interventions

DEVICE

Liberant Thrombectomy System

The Liberant thrombectomy system is indicated for the removal of fresh, soft emboli or thrombi from the vessels of the peripheral arterial and venous systems

Locations (1)

Naples Comprehensive Health

Naples, Florida, United States