Trial Review

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT02480348




Registration number
NCT02480348
Ethics application status
Date submitted
19/06/2015
Date registered
24/06/2015
Date last updated
7/07/2020

Titles & IDs
Public title
Medtronic RevElution Trial
Scientific title
Medtronic Polymer-Free Drug-Eluting Coronary Stent System in De Novo Native Coronary Artery Lesions
Secondary ID [1] 0 0
Version 5.0, 29 JUL 2019
Universal Trial Number (UTN)
Trial acronym
RevElution
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Coronary Artery Disease 0 0
Condition category
Condition code
Cardiovascular 0 0 0 0
Coronary heart disease

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Devices - Polymer-free DES (Drug Eluting Stent)

Experimental: Polymer-free DES (Drug Eluting Stent) -


Treatment: Devices: Polymer-free DES (Drug Eluting Stent)
Intervention code [1] 0 0
Treatment: Devices
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Late lumen loss (LLL, in-stent) at 9 months post-procedure as measured by quantitative coronary angiography.
Timepoint [1] 0 0
9 months

Eligibility
Key inclusion criteria
- Must be an acceptable candidate for percutaneous coronary intervention, stenting, &
emergent coronary artery bypass graft (CABG) surgery

- Must have evidence of ischemic heart disease

- Must require treatment of either a) a single target lesion amenable to treatment with
a 2.25 mm - 3.50 mm stent OR b) two target lesions located in separate target vessels,
with at least one of the target lesions amenable to treatment with a 2.25 mm - 3.50 mm
mm study stent

- Target lesion(s) must be de novo lesion(s) in native coronary artery(ies)
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Known hypersensitivity or contraindication to aspirin, heparin and bivalirudin,
thienopyridines, cobalt, nickel, platinum, iridium, chromium, molybdenum, polymer
coatings (e.g. BioLinx) or a sensitivity to contrast media, which cannot be adequately
pre-medicated

- History of an allergic reaction or significant sensitivity to drugs such as
zotarolimus, rapamycin, tacrolimus, everolimus, or any other analogue or derivative

- History of a stroke or transient ischemic attack (TIA) within the prior 6 months

- Active peptic ulcer or upper gastrointestinal (GI) bleeding within the prior 6 months

- History of bleeding diathesis or coagulopathy or will refuse blood transfusions

- Concurrent medical condition with a life expectancy of less than 5 years

- Currently participating in an investigational drug or another device trial that has
not completed the primary endpoint

- Documented left ventricular ejection fraction (LVEF) < 30% at the most recent
evaluation

Study design
Purpose of the study
Treatment
Allocation to intervention
N/A
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
3/12/2015
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
21/10/2019
Sample size
Target
Accrual to date
Final
109
Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA
Recruitment hospital [1] 0 0
Eastern Heart Clinic - Prince of Wales Hospital - Sydney
Recruitment hospital [2] 0 0
The Prince Charles Hospital - Chermside
Recruitment hospital [3] 0 0
St. Andrew's Hospital - Adelaide
Recruitment hospital [4] 0 0
Royal Adelaide Hospital - Adelaide
Recruitment hospital [5] 0 0
Wesley Hospital / HeartCare Partners - Auchenflower
Recruitment hospital [6] 0 0
Flinders Medical Center - Bedford Park
Recruitment hospital [7] 0 0
St. Vincent's Hospital - Darlinghurst
Recruitment hospital [8] 0 0
Royal Brisbane & Women's Hospital - Herston
Recruitment hospital [9] 0 0
Monash Medical Center - Melbourne
Recruitment hospital [10] 0 0
Northern Hospital - Melbourne
Recruitment hospital [11] 0 0
Fiona Stanley Hospital - Murdoch
Recruitment hospital [12] 0 0
John Hunter Hospital - New Lambton
Recruitment hospital [13] 0 0
Royal North Shore Hospital - St Leonards
Recruitment postcode(s) [1] 0 0
2031 - Sydney
Recruitment postcode(s) [2] 0 0
4032 - Chermside
Recruitment postcode(s) [3] 0 0
5000 - Adelaide
Recruitment postcode(s) [4] 0 0
- Auchenflower
Recruitment postcode(s) [5] 0 0
5042 - Bedford Park
Recruitment postcode(s) [6] 0 0
2010 - Darlinghurst
Recruitment postcode(s) [7] 0 0
4029 - Herston
Recruitment postcode(s) [8] 0 0
3168 - Melbourne
Recruitment postcode(s) [9] 0 0
- Melbourne
Recruitment postcode(s) [10] 0 0
- Murdoch
Recruitment postcode(s) [11] 0 0
- New Lambton
Recruitment postcode(s) [12] 0 0
2065 - St Leonards
Recruitment outside Australia
Country [1] 0 0
Brazil
State/province [1] 0 0
São Paulo
Country [2] 0 0
Singapore
State/province [2] 0 0
Singapore

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Medtronic Vascular
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
The purpose of this trial is to evaluate the clinical safety and efficacy of the Polymer-Free
Drug-Eluting coronary stent system for the treatment of de novo lesions in native coronary
arteries with a reference vessel diameter (RVD) that allows use of stents between 2.25 and
3.50 mm in diameter.
Trial website
https://clinicaltrials.gov/ct2/show/NCT02480348
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT02480348