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PET-CT After Nellix Implantation

R

Rijnstate Hospital

Status

Completed

Conditions

Aortic Aneurysm
Endovascular Repair

Treatments

Device: Nellix Endoprosthesis

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

To determine FDG uptake following uncomplicated EVAR using the Nellix endoprosthesis. Does uncomplicated EVAR using the nellix endoprosthesis result in increased FDG uptake and false positive PET imaging?

Full description

One of the most devastating complications following endovascular aneurysm repair (EVAR) is infection of the used endoprosthesis. Because of the high mortality of secondary surgery following infection, patients with a possible endoprosthesis infection are treated using broadspectrum antibiotics during months, years or even life-long. Unfortunately, the diagnosis of an endoprosthesis infection is difficult and based upon clinical suspicion and non-specific symptoms (e.g. fever and weigth loss) only. Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) is often used as a diagnostic tool to identify infection following EVAR. Like infection, sterile physiologic inflammation following EVAR is also associated with increased metabolism and FDG uptake. This could result in (false-)positive PET imaging resulting in diagnostic errors and antibiotic overuse.

The Nellix endoprosthesis is a relatively new device used for EVAR. In present literature there is no data on the degree of physiologic inflammation following implantation of a Nellix device and the value of postoperative FDG-PET imaging to detect infection is not known. This makes the diagnosis of infection following Nellix implantation extremely difficult. This pilot is designed to determine physiologic FDG uptake following uncomplicated EVAR using the Nellix endoprosthesis.

Enrollment

10 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients treated with Nellix endoprosthesis

Exclusion criteria

  • Diabetes Mellitus (Type 1 and type 2)
  • Current known inflammation or malignancy

Trial design

10 participants in 1 patient group

Treated group
Description:
Patient group treated with Nellix Endoprosthesis.
Treatment:
Device: Nellix Endoprosthesis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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