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Predicting Endoleaks Following Endovascular Aortic Aneurysm Repair Using 18F-Sodium Fluoride

The PET-EVAR Study - Predicting Endoleaks Following Endovascular Aortic Aneurysm Repair Using 18F-Sodium Fluoride

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04577716
Acronym
PET-EVAR
Enrollment
102
Registered
2020-10-08
Start date
2021-04-01
Completion date
2025-03-31
Last updated
2025-07-03

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

Conditions

Abdominal Aortic Aneurysm, Endoleak, Stent-Graft Endoleak

Keywords

EVAR, Endoleak, 18F-Sodium Fluoride, PET

Brief summary

The purpose of the study is to describe Sodium Fluoride uptake (using Positron Emission Tomography-Computed Tomography - PET-CT) following Endovascular Aneurysm Repair (EVAR) and to determine whether Sodium Fluoride PET-CT can predict the development of endoleaks.

Detailed description

Abdominal aortic aneurysms are a leading cause of death in the United Kingdom. Surveillance programmes and pre-emptive surgical repair are lifesaving. Traditional open surgical repair is associated with major perioperative morbidity and mortality and there has been a move towards minimally invasive Endovascular Aneurysm Repair (EVAR), which reduces these early risks. However, the cost effectiveness and long-term clinical effectiveness of EVAR is undermined by concerns of durability due to the development of endoleaks and late aneurysm rupture secondary to progression of native aortic aneurysm disease and stent graft failure. It has previously been demonstrated that 18F-Sodium Fluoride Positron Emission Tomography can predict progression of aneurysm disease and is associated with greater rates of abdominal aortic aneurysm expansion and the future risk of rupture or surgical repair. The investigators here wish to examine whether 18F-Sodium Fluoride on Positron Emission Tomography uptake (i) is increased in patients with endoleaks or related complications, (ii) can prospectively predict the likelihood of developing endoleaks in patients undergoing EVAR, and (ii) is a feasible approach to select patients for EVAR with a reduced future risk of stent graft failure and re-intervention. The investigators believe that there is a compelling scientific rationale for this approach with major translational potential to better select subgroups of patients for EVAR and ultimately improve their outcome.

Interventions

PET scan using the 18F-Sodium Fluoride radiotracer followed by an attenuation correction CT scan

DIAGNOSTIC_TESTCT Aortic Angiogram

CT scan to assess aortic morphology and contextualise PET scan

DIAGNOSTIC_TEST12-month CT Aortic Angiogram

CT scan to assess aortic morphology and the stent graft

OTHER24-month review

This will consist of a telephone consultation with the study participant and review of electronic clinical records

Sponsors

NHS Lothian
CollaboratorOTHER_GOV
NHS Greater Glasgow and Clyde
CollaboratorOTHER
NHS Lanarkshire
CollaboratorOTHER_GOV
NHS Tayside
CollaboratorOTHER_GOV
University of Edinburgh
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* A diagnosis of AAA as defined by the European Society of Vascular Surgery guidelines on the management of aorto-iliac artery aneurysms, and having undergone endovascular repair within the recommended Instructions For Use (IFU) by the manufacturer. \['Endoleak' and 'No Endoleak groups only\] * Complication will be defined as any type of endoleak or stent graft migration \['Endoleak' group only\]. * A diagnosis of AAA requiring endovascular repair OR a diagnosis of juxtarenal AAA requiring fenestrated endovascular aneurysm repair as defined by the European Society of Vascular surgery guidelines on the management of aorto-iliac artery aneurysms and planned EVAR or fenestrated EVAR surgery. \['pre-EVAR' group only\] * Minimum age: 50 years. No maximum age. * Retain capacity for informed consent

Exclusion criteria

* The inability of patients to undergo PET/CT scanning * Chronic kidney disease (eGFR ≤ 30 mL/min/1.73 m2) * Major or untreated cancer * Pregnancy * Allergy or contra-indication to iodinated contrast * Inability or unwillingness to give informed consent * Life-expectancy of less than two years * Known history of connective tissue disease

Design outcomes

Primary

MeasureTime frameDescription
Microcalcification activity in stented and aneurysmal aorta12 monthsWill be measured as 18F Sodium Fluoride binding in the aorta. Uptake will be quantified in Standardised Uptake Values and as a tissue to background ratios.

Secondary

MeasureTime frameDescription
Pattern of microcalcification activity in the stented aorta12 monthsMicrocalcification activity
Intensity of microcalcification activity in the stented aorta12 monthsMicrocalcification activity
Endoleaks12 monthsComputed tomography and ultrasound endpoints
Stent graft migration12 monthsComputed tomography and ultrasound endpoints
Aneurysm sac diameter12 monthsComputed tomography and ultrasound endpoints
Geometry: tortuosity, curvature, torsion12 monthsComputed tomography and ultrasound endpoints
Aneurysm-related mortality24 monthsClinical endpoints
Re-intervention24 monthsClinical endpoints
All-cause mortality24 monthsClinical endpoints
Neck diameter and neck angulation12 monthsComputed tomography and ultrasound endpoints

Other

MeasureTime frameDescription
Co-localisation of 18F-Sodium Fluoride with histological changes in aortic tissue12-36 monthsUptake of 18F-Sodium Fluoride will be identified on PET-CT scans that are acquired as part of the study visit. This will be compared with histological changes in aortic specimens obtained if participant undergoes an open aortic procedure during the study period.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026