Trials / Recruiting
RecruitingNCT05777460
Mid- and Long-term Outcomes of Custom-made Aortic Devices
Results From a Multicenter Registry on the Outcomes of the Terumo Custom-made Aortic Endograft
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (estimated)
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to evaluate mid- and long-term outcomes after Thoracic endovascular aortic repair (TEVAR) with custom-made devices.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Thoracic endovascular aortic repair (TEVAR) | The TEVAR procedure involves the placement of a covered stent (a metal mesh tube with a layer of fabric) into the weakened area of the artery. |
Timeline
- Start date
- 2020-10-01
- Primary completion
- 2025-11-01
- Completion
- 2027-11-01
- First posted
- 2023-03-21
- Last updated
- 2025-03-18
Locations
1 site across 1 country: Italy
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05777460. Inclusion in this directory is not an endorsement.