Trials / Completed
CompletedNCT04620889
LeMaitre LifeSpan® ePTFE Vascular Graft Retrospective Registry
A Retrospective Patient Registry on the Long-Term Safety and Performance of the LifeSpan® ePTFE Vascular Graft Used in Open Vascular Surgery
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 153 (actual)
- Sponsor
- LeMaitre Vascular · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
This is a post-market, single-arm, retrospective registry. The investigator or its representative will identify eligible patients through a medical record search.
Detailed description
This is a post-market, single-arm, retrospective registry. The investigator or its representative will identify eligible patients through a medical record search. Data will be captured retrospectively. Subjects will have been treated with the investigational device in the past and according to standard of care. Subjects will not be involved in any registry related procedures.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AV Access | Arteriovenous shunting for blood access. |
| DEVICE | PVP | Bypass or reconstruction of diseased or occluded blood vessels |
Timeline
- Start date
- 2020-11-27
- Primary completion
- 2023-11-24
- Completion
- 2023-11-24
- First posted
- 2020-11-09
- Last updated
- 2024-10-18
Locations
1 site across 1 country: Germany
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04620889. Inclusion in this directory is not an endorsement.