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Prospective Multicenter Study to Characterize the REAL-WORLD EVIDENCE Regarding Safety and Performance of the Aspiration Catheters Family

NCT05536167 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 57

Last updated 2024-02-01

No results posted yet for this study

Summary

The purpose of this post market study is to collect clinical data of the Arthesys Aspiration catheters family during percutaneous intervention and/or stenting procedure of vessels in the central and peripheral circulation system, including saphenous vein grafts, to support MDR submission.

Conditions

  • Thrombus in the Central and Peripheral Circulatory System, Including Saphenous Vein Grafts

Sponsors & Collaborators

  • Arthesys

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-12
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05536167 on ClinicalTrials.gov