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Not yet recruitingNCT06975215PRIZEUpdated May 16, 2025

Pre-emptive Coil Embolization in Endovascular Aortic Repair

An interventional study of Concomitant embolization and EVAR in Abdominal Aneurysm, Endovascular Aortic Repair and Endoleak, sponsored by Uppsala University. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-05-16.

Sponsored by Uppsala University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
332
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Abdominal aortic aneurysms are often treated with a minimally invasive procedure called endovascular aortic repair (EVAR). While EVAR is widely used, it can sometimes lead to complications over time, and some patients may require further procedures. One of the main issues is endoleak, which occurs when blood continues to flow into the aneurysm sac after treatment. This often happens because small nearby blood vessels, or other sources, continue to supply blood to the aneurysm.

A potentialy strategy to reduce the risk of endoleak is pre-emptive embolization-a technique used during EVAR to block these sources of persistent blood flow. This can include embolization of side branches, the aneurysm sac, or other contributing vessels. Early findings suggest that pre-emptive embolization may lower the risk of endoleaks, but it is still uncertain whether it improves long-term outcomes.

The PRIZE study (Randomized Controlled Trial on Pre-emptive Coil Embolization in Endovascular Aortic Repair) is designed to answer this question. In this research, patients are randomly assigned to one of two groups: one group will receive EVAR with pre-emptive embolization, and the other will receive EVAR without it.

Two main outcomes will be assessed. The first is aneurysm sac regression at two years, meaning a reduction in the size of the aneurysm sac after treatment. This is important because sac shrinkage after EVAR has been linked to lower overall mortality, even though the exact reasons for this are not yet fully understood. The second main outcome is the rate of aortic-related events over five years, as ensuring the long-term durability of treatment is a key goal of this study. Secondary outcomes, including quality of life, patient satisfaction, and cost-effectiveness will also be evaluated.

Currently, there is no clear agreement on whether pre-emptive embolization should be routinely used during EVAR. In a recent international survey, 76% of aortic specialists agreed that more evidence is needed. The PRIZE study aims to provide that evidence. If pre-emptive embolization proves effective, it could become a standard addition to EVAR, helping to improve both the immediate success and long-term durability of treatment. If not, the study will help avoid unnecessary procedures, ensuring patients receive only treatments that offer real benefits.

02

Conditions studied

  • Abdominal Aneurysm
  • Endovascular Aortic Repair
  • Endoleak
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Abdominal aortic aneurysms with a maximum aortic diameter above the threshold for repair level.
  • High-risk criteria for type 2 endoleaks

Exclusion criteria

Exclusion Criteria:

  • Does not fulfill instructions for use for standard EVAR
  • Contraindication for EVAR
  • Life expectancy less than 2 years
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
332 participants (estimated)

Study arms

  • Active comparator
    EVAR

    EVAR, as per standard of care

    Procedure: EVAR

  • Experimental
    EVAR + embolization

    EVAR, as per standard of care, associated with concomitant embolization

    Device: Concomitant embolization · Procedure: EVAR

Interventions

  • DeviceConcomitant embolization

    This will include EVAR, following the standard pathway of care, associated with embolization. The decision to perform side-branch embolization or aneurysm sac embolization will be left to each participating centre/physician.

  • ProcedureEVAR

    Endovascular aortic aneurysm repair

05

What researchers measure

Primary outcomes

  1. Aneurysm sac regression at 2 years

    Changes in the maximum aneurysm sac volume, which will be to assessed by an independent core lab.

    Time frame: 24 months

  2. Rate of aortic events at 5 years

    The number of study participants with aortic events, including: * Aortic-related reinterventions * Development of type I/III, with or without reintervention * Development of T2EL with sac expansion \>10mm with or without reintervention * Graft infection * Aneurysm rupture * Aortic-related death

    Time frame: 60 months

06

Study locations

No study locations are listed for this record.

07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT06975215
Lead sponsor
Uppsala University
Responsible party
Sponsor
First posted
May 16, 2025
Start date
Sep 1, 2025 (estimated)
Primary completion
Sep 1, 2030 (estimated)
Completion
Sep 1, 2033 (estimated)
Last update
May 16, 2025

Study contacts

Carlota F. Prendes, MD, PhD
Contact
carlota.fernandez@uu.se
+46729621501

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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