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Italian Multicenter Database for Open Conversions After EVAR

Italian Multicenter Prospective Database for Open Conversions and SemiConversions After Endovascular Aneurysm Repair

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04299984
Acronym
iConveRt
Enrollment
500
Registered
2020-03-09
Start date
2022-01-01
Completion date
2032-12-31
Last updated
2025-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Aortic Aneurysm, Abdominal Aortic Aneurysm Enlargement

Keywords

Abdominal aortic aneurysm, Open surgical conversion, Endovascular repair, EVAR explantation, Failed EVAR

Brief summary

Late endovascular abdominal aneurysm repair (EVAR) complications not amenable to endovascular correction can undergo either late open conversion (LOC) or semi-conversion (SC). LOC is defined as a total or partial endograft explantation \>30 days after the initial EVAR. SC is defined as open or laparoscopic surgery for endoleak (EL) correction with complete endograft preservation. The aim of this study is to collect in a prospective database the technical aspects of a multicenter experience of LOC and SC, and to analyse early and long-term outcomes of these two treatments.

Interventions

PROCEDUREOpen Conversion after EVAR

See Open Conversions group description.

PROCEDURESemiConversion after EVAR

See SemiConversions group description.

Sponsors

Azienda Ospedaliero-Universitaria di Parma
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* open or laparoscopic surgery for EVAR complications, with or without endograft explantation

Exclusion criteria

* endovascular reinterventions * extra-anatomical bypass surgery (e.g. femoro-femoral crossover bypass) not associated with direct aorta/endograft surgery

Design outcomes

Primary

MeasureTime frameDescription
Early Mortality30 days30-day mortality after surgery
In-hospital Mortality90 daysMortality during in-hospital stay
Long-term survival4 yearsLong-term survival rate

Secondary

MeasureTime frameDescription
Related complications4 yearsAorta-related complications during follow-up
Early Morbidity30 daysMajor complications after surgery

Countries

Italy

Contacts

Primary ContactPaolo Perini, MD
p.perini@live.com+390521702349

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026