- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02360137
Atherosclerotic Plaque Characteristics Associated With a Progression Rate of the Plaque in Carotids and a Risk of Stroke (ANTIQUE)
Atherosclerotic Plaque Characteristics Associated With a Progression Rate of the Plaque and a Risk of Stroke in Patients With the carotId Bifurcation Plaque Study
Study Overview
Status
Conditions
Detailed Description
Objectives and aims The objective of the project is to identify measurable features of atherosclerotic plaque in carotids associated with plaque progression and increased stroke/TIA risk using duplex sonography and digital B-mode image analysis.
The project aims
to identify characteristics of carotic atherosclerotic plaque in ultrasound B-mode associated with a risk of progression or stroke/TIA onset - the "vulnerable" atherosclerotic plaque using
- visual assessment
- digital image analysis using a computer program
to determine the correlation of the ultrasound finding of carotic atherosclerotic plaque in a B-mode in vivo (before endarterectomy) and subsequently in vitro (after endarterectomy) in patients indicated to carotid endarterectomy using
- visual assessment
- digital image analysis using a computer program
to assess a correlation between histological evaluation of composition of atherosclerotic plaque obtained during carotid endarterectomy and ultrasound image of atherosclerotic plaque in a B-mode in vitro using
- visual assessment
- digital image analysis using a computer program
to compare histological and ultrasound findings in vitro and in vivo between asymptomatic and symptomatic atherosclerotic plaques in the carotid bifurcation using
- visual assessment
- digital image analysis using a computer program
to compare the features of asymptomatic and symptomatic atherosclerotic plaque in the carotid bifurcation using
- sonographic perfusion examination of plaque in vivo (after application of echocontrast agent)
- elastography
The grant project is in concordance with the scope, expected benefits, key objective of the Programme "Ensuring internationally comparable levels of healthcare research and use the results to improve the health of Czech population and to secure the current needs of the health sector in the Czech Republic" and the sub-objective 1.2.2. "The development of early diagnosis of cardiovascular and cerebrovascular disease and finding treatment modalities and procedures in the treatment of cardiovascular and cerebrovascular disease with greater therapeutic efficiency and greater parsimony for the patient."
Project design
Patients The project period will take 132 months. Total of 1863 patients with atherosclerotic plaques in the carotid bifurcation and internal carotid artery causing arterial stenosis ≥ 30% detected by duplex sonography will be included to the study. Patients indicated for carotid intervention according to the currently valid guidelines (American Heart Association/American Stroke Association [AHA], European Stroke Organisation [ESO]) will undergo carotid endarterectomy or carotid stenting. Patients will be screened and enrolled in sonographic laboratories of the Military University Hospital in Prague, Na Homolce Hospital Prague, University Hospital Ostrava, Olomouc and Hradec Kralove.
Inclusion criteria: 1/ age 30 - 90 years, 2/ sufficient image quality of atherosclerotic plaque in the carotid bifurcation and ICA using ultrasound, 3/ independency of the patient (0 - 2 points in the modified Rankin scale), 4/ signed informed consent.
Exclusion criteria: 1/ serious disease with a low probability of survival of at least 3 years, 2/ other objective obstacles preventing regular 6-month ultrasound scan.
Clinical examination: Physical and neurological examinations and examinations of carotid arteries by duplex sonography will be performed in all patients at baseline and every 6 months for 3 years.
Sample size calculation The sample size for prospective follow-up of atherosclerotic plaques was based on an expected 5% difference in stroke risk between plaque characteristics. Pre-study calculations showed that a minimum of 1863 patients were needed to reach a significant difference with an alpha value of 0.05 (two-tailed) and a beta value of 0.8 assuming that 20 % of subjects will lost to follow-up.
The sample size for patients undergoing carotid endarterectomy with subsequent in vitro sonographic and histological evaluation of atherosclerotic plaques was based on an expected Spearman's correlation coefficient ≥ 0.3 between histological and sonographic evaluation of atherosclerotic plaque (visual and digital image analysis). Pre-study calculations showed that a minimum of 152 patients were needed to reach a significant difference with an alpha value of 0.01 (after Bonferroni correction for 5 evaluated factors) and a beta value of 0.8 assuming that 20 % of plaques will not be suitable for evaluation.
- Duplex sonographic examination of carotid arteries Standard duplex sonography of cervical vessels focusing on the carotid bifurcation and proximal part of the ICA with measurement of the maximum width of atherosclerotic plaque and transcranial duplex color-coded sonography will be performed in all all patients at baseline and thereafter in 6-month period for 3 years (totally 7 examinations). Examinations will be performed using high-end duplex ultrasound system ESAOTE MyLab Twice (ESAOTE, Genova, Italy) with linear probe LA435 (10 - 18 MHz), vascular preset, scanning depth 4.0 cm, 2 focuses in 2.0 and 3.0 cm; for transcranial duplex sonography, a phase array PA 240 (2 - 4 MHz) will be used. Free hand sonographic scanning will be performed in B-mode in longitudinal and transversal planes (continuous hand moving without changes of probe angle). Video sequences from both longitudinal and transversal scanning and images of cross-section of the plaque in subsequent distance of 0.5 mm will be saved and encoded. Visual characteristics of the plaque (echogenicity, homogeneity, surface, etc.) and digital image analysis using B-mode Assist System will be performed from each video sequence and each cross-section of the plaque. Sonographic examination of plaque perfusion in vivo after application of echocontrast agent (SonoVue, Bracco, Italy) and elastography will be performed in at least 25 patients.
- Carotid endarterectomy Surgery will be undertaken according to standard protocols using general anesthesia in all patients at both centers (with > 400 carotid endarterectomies carried out during the last 5 years). All patients will be on uninterrupted long-term acetylsalicylic acid therapy (100 mg/day) or dual antiplatelat therapy during the perioperative period. A dose of 100 IU per 1 kg of body weight of unfractionated heparin (Heparin Léčiva, Zentiva, k.s., Prague, Czech Republic) will be administered routinely at least 3 - 5 min before flow arrest in carotid artery. The plaque in carotid bifurcation and proximal part of the ICA will be removed as a 1 block from the artery. Protamin (Protamin Meda-Ampullen, Legacy Pharmaceuticals Switzerland GmbH, Birsfelden, Switzerland) in a dose of 1 mL per 2,000 IU of unfractionated heparin will be administered 5 min after flow restoration in the ICA when needed. Clopidogrel (Trombex 75 mg, Zentiva, k.s., Prague, Czech Republic) will be administered 5 days after surgery (75 mg/day) when indicated.
- Sonographic examination of atherosclerotic plaque in vitro All atherosclerotic plaques obtained during endarterectomy as a 1 block will be examined sonographically in vitro. Examination will be performed using the high-end duplex ultrasound system ESAOTE MyLab Twice (ESAOTE, Genova, Italy) with linear probe LA435 (10-18 MHz), vascular preset, scanning depth 2.0 cm, 2 focuses in 1.0 and 2.0 cm. Atherosclerotic plaques extracted from carotid arteries will be transported in a box with formaldehyde. Each plaque will be inserted to the open plastic box filled by HAES 130/04 Voluven solution (colloid plasma expander). Free hand sonographic scanning will be performed in B-mode in longitudinal and transversal planes (continuous hand moving without changes of probe angle). Video sequences from both longitudinal and transversal scanning and images of cross-section of the plaque in subsequent distance of 0.5 mm will be saved and encoded. Visual characteristics of the plaque (echogenicity, homogeneity, surface, etc.) and digital image analysis using B-mode Assist System will be performed from each video sequence and each cross-section of the plaque.
- Histological processing and analysis of atherosclerotic plaque All atherosclerotic plaques obtained during endarterectomy as a 1 block will be processed and analysed histologically after sonographic examination. Visual characteristics of the plaque and digital image analysis using B-mode Assist System will be performed from each cross-section of the plaque.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Czech Republic
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Ostrava, Czech Republic, Czechia, 70852
- University Hospital Ostrava
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- age 30 - 90 years
- sufficient image quality of atherosclerotic plaque in the carotid bifurcation and ICA using ultrasound
- independency of the patient (0 - 2 points in the modified Rankin scale)
- signed informed consent.
Exclusion Criteria:
- serious disease with a low probability of survival of at least 3 years
- other objective obstacles preventing regular 6-month ultrasound scan.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Patients with carotid plaque
Patients with carotid plaque treated using only drugs
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Patients with carotid stenosis
Patients with carotid stenosis indicated to carotid endarterectomy
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Plaque progression
Time Frame: 10 years
|
Sonographic and histological characteristics associated with plaque progression
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10 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sonographic plaque characteristics correlation
Time Frame: 1 year
|
Sonographic plaque characteristics correlation, using Spearman correlation coefficient to verify the existence of correlations between carotid atherosclerotic plaque in a B-mode in vivo (before endarterectomy) and subsequently in a B-mode in vitro (after endarterectomy) in homogeneity, composition, echogenity index, plaque surface type
|
1 year
|
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Histological and sonographic plaque characteristics correlation
Time Frame: 1 year
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Histological and sonographic plaque characteristics correlation, using Spearman correlation coefficient to verify the existence of correlations between variables - homogeneity, composition, echogenity index, plaque surface type
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1 year
|
|
Stroke risk
Time Frame: 10 years
|
Sonographic and histological characteristics associated with stroke or TIA risks, such as homogeneity, composition, echogenity index, plaque surface type
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10 years
|
|
Mortality
Time Frame: 10 years
|
Sonographic and histological characteristics associated with mortality, such as homogeneity, composition, echogenity index, plaque surface type
|
10 years
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: David Skoloudík, MD, Prof, University Hospital Ostrava
Publications and helpful links
General Publications
- Skoloudik D, Kesnerova P, Hrbac T, Netuka D, Vomacka J, Langova K, Herzig R, Belsan T. Risk factors for carotid plaque progression after optimising the risk factor treatment: substudy results of the Atherosclerotic Plaque Characteristics Associated with a Progression Rate of the Plaque and a Risk of Stroke in Patients with the carotid Bifurcation Plaque Study (ANTIQUE). Stroke Vasc Neurol. 2022 Apr;7(2):132-139. doi: 10.1136/svn-2021-001068. Epub 2021 Dec 1.
- Fadrna T, Miksova Z, Herzig R, Langova K, Licman L, Skoloudik D. Factors influencing quality of life in patients followed in the neurosonology laboratory for carotid stenosis. Health Qual Life Outcomes. 2018 Apr 27;16(1):79. doi: 10.1186/s12955-018-0902-2.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 15-29410A
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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