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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT04674969
Registration number
NCT04674969
Ethics application status
Date submitted
1/12/2020
Date registered
19/12/2020
Date last updated
21/08/2024
Titles & IDs
Public title
Drug-Eluting Registry: Real-World Treatment of Lesions in the Peripheral Vasculature
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Scientific title
Drug-Eluting Registry: Real-World Treatment of Lesions in the Peripheral Vasculature (ELEGANCE)
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Secondary ID [1]
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S2444
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Universal Trial Number (UTN)
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Trial acronym
ELEGANCE
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Peripheral Vascular Diseases
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Condition category
Condition code
Cardiovascular
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Diseases of the vasculature and circulation including the lymphatic system
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Intervention/exposure
Study type
Observational [Patient Registry]
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Treatment: Devices - Any eligible commercially available Boston Scientific Corporation (BSC) drug-eluting device.
Clinical Cohort - All enrolled patients are included in the Clinical Cohort. Patients will complete assessments per standard of care through 2-year follow-up in Australia, Austria, Canada, France, Germany, Poland, Spain, Taiwan, Thailand, and the United States. Patients will complete assessments per standard of care through 5-year follow-up in China.
Outcomes Cohort - Patients at select sites will complete the Clinical Cohort standard of care assessments and additional assessments as part of the Outcomes Cohort, including Quality of Life questionnaires, six-minute walk test (6MWT), and Healthcare Utilization data collection.
Treatment: Devices: Any eligible commercially available Boston Scientific Corporation (BSC) drug-eluting device.
Rangerâ„¢ Paclitaxel-Coated Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter; ELUVIAâ„¢ Drug-Eluting Vascular Stent System
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Intervention code [1]
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Treatment: Devices
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Major Adverse Events
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Assessment method [1]
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Rate of MAEs, which include Target Lesion Revascularizations, Major Target Limb Amputations, and Deaths. No pre-specified endpoints or formal tests of hypotheses are proposed. Analyses will be performed for exploratory purposes.
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Timepoint [1]
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12 months
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Primary outcome [2]
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Lesion Patency
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Assessment method [2]
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Lesion patency is determined by Duplex Ultrasound (Investigator and/or Core Lab assessed) and freedom from clinically-driven Target Lesion Revascularization. No pre-specified endpoints or formal tests of hypotheses are proposed. Analyses will be performed for exploratory purposes.
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Timepoint [2]
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12 months
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Eligibility
Key inclusion criteria
* Patients 18 years and older
* Written informed consent (patient data release-form)
* Use of any commercially available Boston Scientific drug-eluting device marketed for treatment of lesions in the peripheral vasculature and specified in the Registry Enrollment Guide
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Life expectancy of <1 year
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
29/03/2021
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
1/01/2028
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Actual
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Sample size
Target
5000
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
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Royal Perth Hospital - Perth
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Recruitment hospital [2]
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Royal North Shore Hospital - St. Leonards
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Recruitment postcode(s) [1]
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6000 - Perth
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Recruitment postcode(s) [2]
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2065 - St. Leonards
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Recruitment outside Australia
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United States of America
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Arkansas
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United States of America
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California
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United States of America
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Connecticut
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Delaware
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District of Columbia
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Florida
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United States of America
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Georgia
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Illinois
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Indiana
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United States of America
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Louisiana
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Massachusetts
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United States of America
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Minnesota
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United States of America
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Mississippi
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New Jersey
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New York
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North Carolina
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Ohio
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Oklahoma
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Pennsylvania
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Texas
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Virginia
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United States of America
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Washington
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Austria
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Graz
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Canada
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Alberta
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Canada
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Quebec
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China
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Beijing
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China
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Chongqing
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China
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Guangdong
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China
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Shandong
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China
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Shanghai
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China
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Shanxi
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China
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Xuhui District
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France
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Le Plessis-Robinson
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France
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Paris
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Germany
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Bruchsal
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Germany
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Essen
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Germany
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München
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Poland
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Poznan
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Spain
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Sabadell
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Taiwan
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Taichung
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Taiwan
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Taipei City
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Thailand
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Bangkok
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Thailand
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Hat Yai
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Boston Scientific Corporation
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
The ELEGANCE Registry's objective is to collect Real-World Data (RWD), including populations previously not represented in Peripheral Vascular Disease (PVD) trials, health economics data, and to support the safe use of commercially available Boston Scientific Corporation (BSC) drug-eluting devices for the treatment of lesions located in the peripheral vasculature.
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Trial website
https://clinicaltrials.gov/study/NCT04674969
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Yumna Akhtar, MS
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Address
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Phone
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651-399-6775
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Fax
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Email
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[email protected]
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT04674969
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