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CARotid plaqUe StabilizatiOn and Regression With Evolocumab. (CARUSO)

Primary Purpose

Carotid Artery Disease

Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Evolocumab
lipid-lowering therapy (LLT)
Sponsored by
Azienda Ospedaliera Ordine Mauriziano di Torino
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Carotid Artery Disease

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

asymptomatic patients with uni- or bilateral carotid artery stenosis ≥50% and LDL-C values ≥100 mg/dL despite ongoing lipid lowering therapy

Exclusion Criteria:

  • age <18 or ≥81 years old
  • known intolerance to evolocumab
  • ongoing or previous treatment with PCSK9i
  • prior stroke or transient ischemic attack
  • total carotid occlusion
  • major active infection or major hematologic, renal, hepatic, or endocrine dysfunction
  • malignancy with life expectancy below 24 months
  • failure to sign informed consent

Sites / Locations

  • Azienda Ospedaliera Ordine Mauriziano di TorinoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Evolocumab

Standard

Arm Description

Subcutaneous evolocumab 140 mg will be administered every 2 weeks on top of optimal lipid-lowering therapy

No further treatment besides optimal lipid-lowering therapy will be administered

Outcomes

Primary Outcome Measures

Morphological carotid plaque stabilization
Morphological stabilization of the carotid plaque evaluated with Carotid duplex ultra-sonography
Carotid plaque regression
Carotid plaque regression evaluated with Carotid duplex ultra-sonography and defined as reduction of the entity of the stenosis and/or peak systolic velocity by at least 5%, as compared to baseline.

Secondary Outcome Measures

Changes of LDL-C
Absolute changes of LDL-C
Major adverse cerebrovascular events
All-cause mortality, cardiovascular mortality, stroke, myocardial infarction, any coronary or peripheral revascularization

Full Information

First Posted
January 24, 2021
Last Updated
July 22, 2021
Sponsor
Azienda Ospedaliera Ordine Mauriziano di Torino
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1. Study Identification

Unique Protocol Identification Number
NCT04730973
Brief Title
CARotid plaqUe StabilizatiOn and Regression With Evolocumab.
Acronym
CARUSO
Official Title
CARotid plaqUe StabilizatiOn and Regression With Evolocumab: the CARUSO Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
March 31, 2022 (Anticipated)
Study Completion Date
March 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliera Ordine Mauriziano di Torino

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The CARUSO trial aims at investigating the efficacy of evolocumab in promoting carotid plaque morphological stabilization and regression as compared to traditional lipid lowering therapy (LLT). Primary end-point of the study is the superiority of evolocumab on top of ongoing LLT versus ongoing LLT in carotid plaque morphological stabilization and regression at 6 and 12 months, respectively. Secondary end-points are: LDL-Cholesterol (LDL-C) absolute and percentage changes in the two groups at 12 month follow-up, and adverse cerebrovascular and cardiac events at 12 and 24 months
Detailed Description
Optimal lipid-lowering therapy (LLT) is a mainstay for the therapeutic management of atherosclerotic vascular disease. Cardiac and cerebrovascular adverse events and progression of atherosclerosis are, indeed, reduced in proportion to the achieved LDL cholesterol (LDL-C) levels.In addition, regression of atherosclerotic plaques with optimal LLT has been observed. However, optimal LLT with statin and ezetimibe, might be limited by the onset of adverse effects (i.e. disabling myalgias, diarrhea) with are usually dose -dependent, and the maximum tolerated statin dose might be insufficient to reach the recommended LDL-C goals. The advent of proprotein convertase subtilisin kexin type 9 inhibitors (PCSK9i) has allowed the achievement of very low LDL-C levels, and the fulfillment of the recommended LDL-C targets. However, while the experience with PCSK9i in patients with coronary artery disease has been wide, and coronary plaque regression has been documented, little is known regarding carotid plaque regression following therapy with PCSK9i. Only a few case reports have been published, and no observational study has been carried out so far. Furthermore, morphological carotid plaque stabilization has a prognostic role, and the possibility of its early achievement with PCSK9i may be relevant, especially in the context of percutaneous or surgical carotid interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carotid Artery Disease

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
randomized controlled study
Masking
InvestigatorOutcomes Assessor
Masking Description
Single blinded study
Allocation
Randomized
Enrollment
130 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Evolocumab
Arm Type
Active Comparator
Arm Description
Subcutaneous evolocumab 140 mg will be administered every 2 weeks on top of optimal lipid-lowering therapy
Arm Title
Standard
Arm Type
Placebo Comparator
Arm Description
No further treatment besides optimal lipid-lowering therapy will be administered
Intervention Type
Drug
Intervention Name(s)
Evolocumab
Other Intervention Name(s)
Repatha
Intervention Description
Evolocumab 140 mg s.c. every two weeks on top of optimal lipid lowering therapy
Intervention Type
Other
Intervention Name(s)
lipid-lowering therapy (LLT)
Intervention Description
lipid-lowering therapy (LLT)
Primary Outcome Measure Information:
Title
Morphological carotid plaque stabilization
Description
Morphological stabilization of the carotid plaque evaluated with Carotid duplex ultra-sonography
Time Frame
Six months
Title
Carotid plaque regression
Description
Carotid plaque regression evaluated with Carotid duplex ultra-sonography and defined as reduction of the entity of the stenosis and/or peak systolic velocity by at least 5%, as compared to baseline.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Changes of LDL-C
Description
Absolute changes of LDL-C
Time Frame
12 months
Title
Major adverse cerebrovascular events
Description
All-cause mortality, cardiovascular mortality, stroke, myocardial infarction, any coronary or peripheral revascularization
Time Frame
12 and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: asymptomatic patients with uni- or bilateral carotid artery stenosis ≥50% and LDL-C values ≥100 mg/dL despite ongoing lipid lowering therapy Exclusion Criteria: age <18 or ≥81 years old known intolerance to evolocumab ongoing or previous treatment with PCSK9i prior stroke or transient ischemic attack total carotid occlusion major active infection or major hematologic, renal, hepatic, or endocrine dysfunction malignancy with life expectancy below 24 months failure to sign informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tiziana Claudia Aranzulla, MD
Phone
+390115085038
Email
taranzulla@mauriziano.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tiziana Claudia Aranzulla, MD
Organizational Affiliation
A.O. Ordine Mauriziano di Torino
Official's Role
Principal Investigator
Facility Information:
Facility Name
Azienda Ospedaliera Ordine Mauriziano di Torino
City
Torino
State/Province
Piedmont
ZIP/Postal Code
10134
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tiziana Claudia Aranzulla, MD
Phone
+393383145483
Email
aranzulla.tiziana@gmail.com
First Name & Middle Initial & Last Name & Degree
Irene Borsotti
Phone
+390115082222
Email
lborsotti@mauriziano.it
First Name & Middle Initial & Last Name & Degree
Tiziana Claudia Aranzulla, MD, MSc
First Name & Middle Initial & Last Name & Degree
Salvatore Piazza, MD
First Name & Middle Initial & Last Name & Degree
Andrea Ricotti, MD
First Name & Middle Initial & Last Name & Degree
Giuseppe Musumeci, MD
First Name & Middle Initial & Last Name & Degree
Andrea Gaggiano, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33893754
Citation
Aranzulla TC, Piazza S, Ricotti A, Musumeci G, Gaggiano A. CARotid plaqUe StabilizatiOn and regression with evolocumab: Rationale and design of the CARUSO study. Catheter Cardiovasc Interv. 2021 Jul 1;98(1):E115-E121. doi: 10.1002/ccd.29743. Epub 2021 Apr 24.
Results Reference
result

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CARotid plaqUe StabilizatiOn and Regression With Evolocumab.

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