Interest of a Post-operative Ultrasound With Systematic Use of Ultrasonic Contrast in the Follow-up of Aortic Endoprosthesis: Prospective Study at the University Hospital of Nice
Ultra_Evar
1 other identifier
interventional
40
1 country
1
Brief Summary
This is a prospective study conducted on a population with an aortic endoprosthesis in the context of an abdominal aortic aneurysm. The study's objective is to standardize the ultrasound methodology in the monitoring of aortic endoprosthesis in immediate post-operative care by comparing the results with CT-scan (gold standard). To improve ultrasound methodology, the investigators propose to use the VESMA protocol for ultrasound diameter measurement at four incidences. In addition, the use of ultrasonic contrast agents increases the accuracy of vascular structures, the quality of the ultrasound blood flow image and the duration of signal enhancement. This makes it possible to visualize small gauge vessels and those with slow flows. In this way, the investigators could improve the ultrasound technique for measuring aneurysm bag diameters and endoleak detection. Moreover, the toxicity of iodinated contrast agents is the third cause of acute renal failure in hospitalized patients and is all the more frequent when the investigators increase injections. Improving the quality of ultrasound investigations for the monitoring of aortic endoprosthesis would therefore allow us to reduce the number of CT-scan performed in this population and thus reduce irradiation and the injection of nephrotoxic products. Thereby, the investigators would like to integrate the technique into the systematic follow-up of patients who have benefited from the placement of an aortic endoprosthesis by replacing the CT-scan.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2020
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 13, 2019
CompletedFirst Posted
Study publicly available on registry
December 12, 2019
CompletedStudy Start
First participant enrolled
February 28, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 10, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
December 10, 2022
CompletedMarch 24, 2026
March 1, 2026
1.8 years
November 13, 2019
March 20, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
measurement of anterior-posterior diameters according to 4 aortic endoprosthesis incidences after PCUS injection in immediate post-operative
1 day
detection of endoleaks after PCUS injection in immediate post-operative
1 day
measurement of anterior-posterior diameters of endoleaks after PCUS injection in immediate post-operative
1 day
Secondary Outcomes (4)
Description of endoleaks after PCUS injection in immediate post-operative
1 day
Description of exit doors of heart after PCUS injection in immediate post-operative
1 day
Description of their flows after PCUS injection in immediate post-operative
1 day
Description of maximum circulatory speeds after PCUS injection in immediate post-operative
1 day
Study Arms (1)
écho-doppler with ultrasonar Sonovue® injection
EXPERIMENTALInterventions
During this unique visit they will benefit from 2 imaging exams performed by two different operators: * Echo-doppler without "standard method" contrast injection (common practice) * An echo-doppler with Sonovue® ultrasound injection "Ultra\_evar method" (2.5 ml bolus 2-3 seconds) During this examination, the endoprosthesis and the aneurysm sac will be scanned according to the 4 incidences described above in order to objective whether or not there is a endoleak. The patient then performs the control CT-scan prior to discharge from hospital. The results of the medical imaging exams will be communicated to them before the hospital discharge, once the CT-scan has been performed. A cross-review of the studies will be performed later.
Eligibility Criteria
You may qualify if:
- Patients over 18 years of age.
- Abdominal aortic aneurysm treated with aortic stent.
- Signature of informed consent.
- Person affiliated or beneficiary of a social security scheme
You may not qualify if:
- Hypersensitivity to sulphur hexafluoride or to these excipients (Macrogol 4000, Distearoylphosphatidylcholine, Dipalmitoylphosphatidylglycerol sodé, Palmitic acid).
- Right-left shunt patient
- Patient with severe pulmonary hypertension (pulmonary blood pressure \> 90 mm Hg),
- Patient with uncontrolled systemic hypertension
- Adult patients with respiratory distress syndrome.
- Dobutamine patient in patients with a pathology suggesting cardiac instability
- Hypercoagulation, recent thromboembolic accident
- Fenestrated aortic stent
- Pregnant or nursing woman.
- Severe heart failure.
- Person deprived of liberty by judicial or administrative decision.
- Person subject to legal protection.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital of Nice
Nice, 06000, France
Related Publications (4)
Johnston KW, Rutherford RB, Tilson MD, Shah DM, Hollier L, Stanley JC. Suggested standards for reporting on arterial aneurysms. Subcommittee on Reporting Standards for Arterial Aneurysms, Ad Hoc Committee on Reporting Standards, Society for Vascular Surgery and North American Chapter, International Society for Cardiovascular Surgery. J Vasc Surg. 1991 Mar;13(3):452-8. doi: 10.1067/mva.1991.26737.
PMID: 1999868BACKGROUNDManning BJ, Kristmundsson T, Sonesson B, Resch T. Abdominal aortic aneurysm diameter: a comparison of ultrasound measurements with those from standard and three-dimensional computed tomography reconstruction. J Vasc Surg. 2009 Aug;50(2):263-8. doi: 10.1016/j.jvs.2009.02.243.
PMID: 19631858BACKGROUNDBredahl KK. Response to commentary on "Re: Contrast Enhanced Ultrasound can Replace Computed Tomography Angiography for Surveillance After Endovascular Aortic Aneurysm Repair". Eur J Vasc Endovasc Surg. 2017 Mar;53(3):446-447. doi: 10.1016/j.ejvs.2016.12.029. Epub 2017 Jan 26. No abstract available.
PMID: 28131537BACKGROUNDAmrani S, Eveilleau K, Fassbender V, Obeid H, Abi-Nasr I, Giordana P, Hallab M, Leftheriotis G. Assessment of the systolic rise time by photoplethysmography in peripheral arterial diseases: a comparative study with ultrasound Doppler. Eur Heart J Open. 2022 Apr 28;2(3):oeac032. doi: 10.1093/ehjopen/oeac032. eCollection 2022 May.
PMID: 35919340RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Pascal GIORDANA, MD
Centre Hospitalier Universitaire de Nice
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 13, 2019
First Posted
December 12, 2019
Study Start
February 28, 2020
Primary Completion
December 10, 2021
Study Completion
December 10, 2022
Last Updated
March 24, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share