Contrast Enhanced Ultrasound Endoleak Identification and Classification
NCT ID: NCT04615559
Last Updated: 2022-11-14
Study Results
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Basic Information
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WITHDRAWN
NA
INTERVENTIONAL
2020-12-31
2023-07-31
Brief Summary
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Detailed Description
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Rationale: The most commonly accepted tool for follow up is Computed Tomography (CT) scan which involves ionizing radiation and potentially nephrotoxic iodinated contrast. Routine ultrasound with Doppler, CT, and MRI has all been employed utilizing various imaging protocols. Concerns over cost, potential nephrotoxicity of contrast agents and repeated radiation exposure has led to investigation of alternate imaging modalities such as contrast enhanced ultrasound (CEUS). CEUS also allows continuous (dynamic) or real-time monitoring of the aneurysm and endoleak throughout the study.
Objectives:
Aim 1: To determine the consistency/discrepancy of endoleak detection (positive/negative) for contrast enhanced ultrasound (CEUS) versus various phases of CTA versus delayed phase CTA.
Aim 2 (Exploratory): To explore the consistency/discrepancy of endoleak type (type 1-5) between CEUS and delayed phase CTA.
Aim 3 (Exploratory): To explore the consistency/discrepancy of endoleak source detected (positive/negative for each source) for type II endoleaks between CEUS and CTA.
Aim 4 (Exploratory): Re-assess Aims 1-3 for the follow-up scans. The goal for this aim is to examine whether the consistency/discrepancy patterns discovered in Aims 1-3 can be repeated at the follow-up scans.
Population: 40 patients who have undergone an EVAR or FEVAR for abdominal aortic aneurysms and are expected to have CTA as part of their standard of care will be enrolled in the study.
Methodology: Patients will be evaluated with research contrast ultrasound at one month post-op, six months post-op and at one year.
Data Analysis Plan: Binomial 95% confidence interval will be calculated for sensitivity and specificity. One- sided binomial test will be conducted to test whether the target sensitivity and specificity are superior to the null value, e.g. a minimal acceptable level of sensitivity and specificity. In detecting the rate of endoleak positive on CEUS or other phases of the CTA but negative on CTA in the delayed phase, we will compute Clopper Pearson Exact 95% confidence interval since such a rate could be small. To assess consistency of endoleak type (type 1-5) between CEUS and delayed phase CTA, Kappa coefficient will be used. In the situation with high agreement biased towards one endoleak type, or extremely unbalanced distribution of endoleak types, prevalence-adjusted bias-adjusted kappa coefficient (PABAK) (Byrt, Bishop, and Carlin 1993) will be used. The discrepancy of endoleak type between CEUS and delayed phase CTA will be reported as rate, for example percent of case rated as type 1 in CTA but type 2 in delayed phase, with Clopper Pearson Exact 95% confidence interval. SAS9.4 will be used for all statistical analyses.
Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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contrast enhanced ultrasound
CEUS will be performed at one month post-op, six months post-op and at one year.
Contrast enhanced ultrasound
CEUS involves the use of microbubble contrast agents and specialized imaging techniques to enhance the signal from blood, thus showing flow in macroscopic vessels as well as tissue perfusion information
Interventions
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Contrast enhanced ultrasound
CEUS involves the use of microbubble contrast agents and specialized imaging techniques to enhance the signal from blood, thus showing flow in macroscopic vessels as well as tissue perfusion information
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Unable to receive CEUS contrast, previous reaction to Ultrasound Contrast Agent (UCA)
* BMI \>50
18 Years
ALL
No
Sponsors
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University of Southern California
OTHER
Responsible Party
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Edward Grant
Professor of Clinical Radiology
Principal Investigators
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Edward Grant
Role: PRINCIPAL_INVESTIGATOR
University of Southern California
Locations
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USC Department of Radiology
Los Angeles, California, United States
Countries
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Other Identifiers
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HS-20-00428
Identifier Type: -
Identifier Source: org_study_id
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