Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

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 registered on ANZCTR


Registration number
ACTRN12622000071729p
Ethics application status
Submitted, not yet approved
Date submitted
23/11/2021
Date registered
21/01/2022
Date last updated
21/01/2022
Date data sharing statement initially provided
21/01/2022
Type of registration
Prospectively registered

Titles & IDs
Public title
First in Human Early Feasibility study of BD(TM) Sirolimus Drug Coated Balloon Catheter for Treatment of Femoropopliteal Arteries
Scientific title
A Prospective, Multicenter, Single Arm, Non-Randomized, Study to Assess the Performance and Safety of BD (TM) Sirolimus Drug Coated Balloon Catheter for Treatment of Femoropopliteal Arteries
Secondary ID [1] 305840 0
BDPI-20-012
Universal Trial Number (UTN)
Trial acronym
PREVISION
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Peripheral Artery Disease 324380 0
Femoropopliteal lesions 324381 0
Superficial Femoral Artery lesions 324382 0
Condition category
Condition code
Cardiovascular 321866 321866 0 0
Diseases of the vasculature and circulation including the lymphatic system

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The BD (TM) Sirolimus Drug Coated Balloon Catheter consists of an over-the-wire (OTW) percutaneous transluminal angioplasty balloon catheter coated with sirolimus on the surface of the balloon. The procedure will use angiogram imaging while a interventional radiologist or vascular surgeon delivers the investigational device. This procedure is expected to take approximately 60 minutes. This is a one time intervention during participation of this clinical trial. In order to evaluate the success of this intervention, angiogram imaging will be done at six month follow up visit. this adherence is considered outside of normal standard of care operations.
Intervention code [1] 322243 0
Treatment: Devices
Comparator / control treatment
No Control group - Single arm study
Control group
Uncontrolled

Outcomes
Primary outcome [1] 329622 0
Late Lumen Loss (LLL) of the target lesion, as measured by Quantitative Vascular Angiography (QVA) at 6 Months
Timepoint [1] 329622 0
6 months post interventional angioplasty with the BD(TM) Sirolimus Drug Coated Balloon.
Secondary outcome [1] 403201 0
A Safety Composite comprised of the following data points will be collected through patient medical records and patient reporting at follow up visits.
Composite of freedom from device and procedure related death. Freedom from major target limb amputation (above the ankle). Freedom from all-cause MACE. Freedom from all-cause death through.
Timepoint [1] 403201 0
30-days post angioplasty: Composite of freedom from device and procedure related death through
6, 12, 24 months post angioplasty: Freedom from major target limb amputation (above the ankle). Freedom from all-cause MACE. Freedom from all-cause death.

Eligibility
Key inclusion criteria
Greater than or equal to 18 years of age
Rutherford Clinical Category 2-4
Lesion greater than or equal to 70% stenosis by visual estimate
Lesion Length greater than or equal to 3 cm and less than or equal to 17 cm
Target reference vessel diameter of 5-6 mm and able to be treated with available device size matrix
Minimum age
18 Years
Maximum age
90 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Less than or equal to 90 years of age
Life expectancy of less than 2 years
Participant has acute limb ischemia
Severe Calcification as defined as PARC scoring system
Participant is currently participating in an investigational drug or device study, or previously enrolled in a trial within the last 30 days prior to screening.

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
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
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
28/03/2022
Actual
Date of last participant enrolment
Anticipated
30/09/2022
Actual
Date of last data collection
Anticipated
30/09/2024
Actual
Sample size
Target
50
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA
Recruitment outside Australia
Country [1] 24342 0
New Zealand
State/province [1] 24342 0

Funding & Sponsors
Funding source category [1] 310198 0
Commercial sector/Industry
Name [1] 310198 0
Becton, Dickinson and Company (BD)
Country [1] 310198 0
United States of America
Primary sponsor type
Commercial sector/Industry
Name
Becton, Dickinson and Company (BD)
Address
BD Australia Head Office
BD
Level 5
66 Waterloo Road
Macquarie Park
NSW, 2113
Country
Australia
Secondary sponsor category [1] 311286 0
None
Name [1] 311286 0
Address [1] 311286 0
Country [1] 311286 0

Ethics approval
Ethics application status
Submitted, not yet approved
Ethics committee name [1] 309877 0
Bellberry Human Research Ethics Committee E
Ethics committee address [1] 309877 0
Ethics committee country [1] 309877 0
Australia
Date submitted for ethics approval [1] 309877 0
07/12/2021
Approval date [1] 309877 0
Ethics approval number [1] 309877 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 115702 0
Prof Andrew Holden
Address 115702 0
Vascular Interventional Research Unit, Vascular Service, Level 4, Building 32, Park Road, Grafton, Auckland, New Zealand 1023
Country 115702 0
New Zealand
Phone 115702 0
+64 9 307 4949
Fax 115702 0
Email 115702 0
[email protected]
Contact person for public queries
Name 115703 0
Kaitlynn Wernsing
Address 115703 0
BD
850 West Rio Salado Parkway
Tempe, AZ
85281
Country 115703 0
United States of America
Phone 115703 0
+1 6028305675
Fax 115703 0
Email 115703 0
[email protected]
Contact person for scientific queries
Name 115704 0
Kaitlynn Wernsing
Address 115704 0
BD
850 West Rio Salado Parkway
Tempe, AZ
85281
Country 115704 0
United States of America
Phone 115704 0
+1 6028305675
Fax 115704 0
Email 115704 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.