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VIP - Vascular Infection Project (Cohorte VIP)

U

University Hospital of Bordeaux

Status

Enrolling

Conditions

Infections
Vascular Graft Infection
Aortitis
Blood Vessel Prosthesis

Study type

Observational

Funder types

Other

Identifiers

NCT06866535
CHUBX 2022/01

Details and patient eligibility

About

Constitution of a prospective multicentric observational database to study vascular infections, both native, especially aortitis, and vascular graft and endograft infections. Clinical and paraclinical data on medical, surgical, anesthetic and intensive care management will be collected in order to better characterize these infections

Full description

Vascular infections are rare but severe, burdened by high morbi-mortality and recurrence rates. However, many questions remain regarding their management which is still not consensual, both surgical and medical management. The term "vascular infections" encompasses vascular graft and endograft infections, as well as infections of native arteries and the aorta. For vascular graft infections, the optimal surgery is to remove the infected graft before vascular reconstruction with a new graft, either synthetic or biologic. However, some patients are too fragile to undergo surgery and might then benefit from an endovascular graft, an abscess drainage or no surgery at all, only medical treatment. For native arterial infections, surgery is often required to remove the infected arterial wall before vascular reconstruction. However, some patients cannot be operated on and might also benefit from an endovascular surgery. In these two vascular infections, the ideal anti-microbial treatment is uncertain, whether it pertains to the duration of therapy, the type of molecules, or their number. All of these medical and surgical factors may impact the prognosis of patients and should be collectively assessed in order to determine the best strategy for enhancing their outcomes.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥ 18 years-old;
  • all patients with a vascular infection, either native (aortitis, arteritis) or prosthetic (vascular graft, endograft and/or stent),
  • oral consent

Exclusion criteria

  • patient under legal protection

Trial design

1,000 participants in 2 patient groups

Native vascular infection
Prosthetic vascular infections

Trial contacts and locations

1

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Central trial contact

Mathilde Puges, MD

Data sourced from clinicaltrials.gov

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