LeMaitre LifeSpan® ePTFE Vascular Graft Retrospective Registry

NCT04620889 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 153

Last updated 2024-10-18

No results posted yet for this study

Summary

This is a post-market, single-arm, retrospective registry. The investigator or its representative will identify eligible patients through a medical record search.

Conditions

  • Diseased or Occluded Blood Vessels
  • Arteriovenous Shunting for Blood Access

Interventions

DEVICE

AV Access

Arteriovenous shunting for blood access.

DEVICE

PVP

Bypass or reconstruction of diseased or occluded blood vessels

Sponsors & Collaborators

  • LeMaitre Vascular

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-11-27
Primary Completion
2023-11-24
Completion
2023-11-24
FDA Device
Yes

Countries

  • Germany

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 NCT04620889 on ClinicalTrials.gov