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RECRUITING
NCT05386277
NA

A PMCF Study to Confirm the Performance and Safety of the LeMaitre® TufTex Single Lumen Embolectomy Catheter

Sponsor: LeMaitre Vascular

View on ClinicalTrials.gov

Summary

A post market clinical study to confirm the performance and safety of the LeMaitre® TufTex Single Lumen Embolectomy Catheter on patients undergoing surgical treatment for the removal of arterial emboli and/or thrombi

Official title: A Post Market Clinical Study to Confirm the Performance and Safety of the LeMaitre® TufTex Single Lumen Embolectomy Catheter on Patients Undergoing Surgical Treatment for the Removal of Arterial Emboli and/or Thrombi

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

112

Start Date

2022-01-11

Completion Date

2027-06

Last Updated

2024-10-18

Healthy Volunteers

No

Interventions

DEVICE

TufTex Single Lumen Embolectomy Catheter

The SLC Embolectomy Catheter is indicated for the removal of arterial emboli and thrombi

Locations (3)

Ziekenhuis Oost-Limburg

Genk, Belgium

Andrej Udelnow

Brandenburg, Germany

Giorgio Prouse

Lugano, Switzerland