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The NEXUS™ Compassionate Use Data Collection Study

NCT03420066 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7

Last updated 2024-01-05

No results posted yet for this study

Summary

A Multicenter, observational Data Collection Study to Evaluate the Safety and Performance of the Nexus™ Aortic Arch Stent Graft System in patients that were implanted with the device as part of Compassionate Use Procedures.

Conditions

  • Aortic Arch Aneurysm

Interventions

OTHER

Retrospective data collection

Retrospective collection of data recorded as standard of care for patients that were implanted with the Nexus device as part of Compassionate Use duly authorized according to country specific regulations.

Sponsors & Collaborators

  • Endospan Ltd.

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-19
Primary Completion
2018-09-14
Completion
2023-11-28

Countries

  • Italy
  • New Zealand
  • Switzerland

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 NCT03420066 on ClinicalTrials.gov