Renal Artery StenosisARTISANNCT01673373
Renal Stent Placement for the Treatment of Renal Artery Stenosis in Patients With Resistant Hypertension
A study testing iCAST™ Rx Stent System in people with Renal Artery Stenosis and Hypertension, Renovascular, run by Atrium Medical Corporation at 12 sites in United States.
Trial summary
The purpose of this trial is to test how well the iCAST™ RX Stent works in patients diagnosed with atherosclerotic renal artery stenosis and whether or not increased blood flow by the stent will help to control blood pressure. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Renal Artery Stenosis, Hypertension, Renovascular
- What is being tested?
- iCAST™ Rx Stent System
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 68 participants
- Where
- 12 sitesUnited States
- Study dates
- 23 Oct 2012to 26 Oct 2020
- Phase
- Interventional
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
General Inclusion Criteria:
- Age ≥ 18 at the time of informed consent.
- Subject or subject's legal representative have been informed of the nature of the trial, agrees to participate, and has signed an Institutional Review Board (IRB)/Ethics Committee (EC) approved Informed Consent Form (ICF).
- Subjects that have bilateral kidneys or a solitary functioning kidney with Renal Artery Stenosis in at least one kidney and an average Systolic Blood Pressure (SBP) ≥ 155mmHg.
- Subject has a history of maximum tolerable dose of ≥ 3 anti-hypertensive medications of different classes, one of which must be a diuretic (for at least two weeks prior to Medical Documentation Screening period).
- A documented history for a minimum of 3 months showing reasonable and aggressive efforts to manage hypertension prior to consent. This must include the use of a broad variety of medications that have been used and failed or not tolerated.
- Subject must have documented clinical evidence to support likelihood of angiographic findings > 80% whether it is DUS, CTa, MRa or other medical evidence.
- New York Heart Association (NYHA) class I, II, or III the time of trial enrollment.
Note: When a subject has bilateral Renal Artery Stenosis both of which require stenting, it is recommended to treat both kidneys with an iCAST™ RX Stent System during the index procedure. In the event that a subject needs a renal stenting procedure staged for renal protection, it is important that the Investigator treats the second renal artery with an iCAST™ RX Stent System after 30 days of the index procedure. If subjects with bilateral stenosis have only one lesion that meets protocol inclusion criteria that lesion should be treated per protocol. The recommendation is to NOT treat the second non-qualifying lesion, however if the operator feels strongly it is indicated, then they should treat per standard of care after 30-days post index procedure in order to comply with exclusion criteria #10.
Subjects with flash pulmonary edema are allowed into the trial should they meet all other Inclusion and Exclusion criteria.
Angiographic Anatomic Inclusion Criteria:
- Angiographic diameter renal artery stenosis ≥ 80% involving unilateral or bilateral renal arteries.
- The degree of percent diameter stenosis for all lesions intended to be treated, must be confirmed via one of the following methods: i. Manual or automated measurement with calipers ii. Measured Flow Fraction Reserve (FFR) < 0.8 using a pressure wire iii. Measured translesional peak pressure gradient of > 21 mmHg after induced hyperemia via dopamine or papaverine using a 4 Fr or less catheter or pressure wire.
- Subjects with 60-79% angiographic stenosis who have confirmed FFR < 0.8 may be enrolled.
- Renal pole-to-pole length > 8cm (per visual estimate).
- Target lesion length ≤ 16mm per vessel (per visual estimate).
- Renal artery vessel diameter ≥ 5.0mm and ≤ 7.0mm (per visual estimate).
- Lesion originating ≤ 15mm of the renal ostium.
General Exclusion Criteria:
- Subject's estimated life expectancy is < 12 months.
- Subject has a history of transplanted kidney(s), has had another recent organ transplant or polycystic kidney disease.
- Subject with estimated glomerular filtration rate (eGFR) ≤ 25 mL/min/1.73 m2
- Subject has a history of bleeding diathesis or coagulopathy or refuses blood transfusions.
- Subject has a known contraindication to heparin, aspirin, thienopyridine, other anti-coagulant/antithrombotic therapies, contrast media, stainless steel, and/or polytetrafluoroethylene (PTFE).
- Subject has had a previous renal bypass operation, a bypass is planned, or the target lesion is located within or beyond a bypass graft.
- Subject has received a thrombolytic agent within the past 30 days.
- Subject has documented acute pulmonary edema or systolic heart failure with ejection fraction < 30% and/or hospitalization requiring intubation and ventilation support for this diagnosis within the previous 90 days or hypertensive emergencies defined as resulting in organ damage.
- Concurrent enrollment in any investigational trial wherein subject's participation has not been completed.
- Subject has had a planned or anticipated cardiovascular surgical or interventional procedure outside of the affected renal artery (including, but not limited to, aortic, renal, cardiac, carotid, femoro-popliteal, and below the knee) within 30 days prior to the index procedure and prior to completion of the 30 day follow-up.
- Subject has suffered a stroke or Transient Ischemic Attack (TIA) in the past 3 months.
- Subject is pregnant, lactating, or is of child-bearing potential and plans to become pregnant during the follow-up trial period.
- Subject with significant valvular disease.
- Subject with known significant proteinuria > 2+ or > 2.0gm/d.
- Subject with known bilateral upper-extremity arterial stenosis that result in spuriously low arm pressures or without the ability to gain reliable blood pressure measurements in at least one upper extremity.
- Subject with active sepsis.
- Subject with serum creatinine ≥ 3.0mg/dL.
- Subject with NYHA Class IV at the time of enrollment.
- Subject is on hemodialysis.
- Subject has a history of renal aneurysm.
- Subject with cardiogenic shock.
- Subject with cardiomyopathy.
- Subject has an uncontrolled concurrent illness, including but not limited to ongoing or active infection or active autoimmune disease requiring immunosuppressive therapy.
- Any subject with clinically significant cardiovascular, respiratory, neurologic, hepatic, endocrine, major systematic disease, making implementation or interpretation of the protocol or protocol results difficult or who in the opinion of the investigator would not be a good candidate for enrollment.
Angiographic Anatomic Exclusion Criteria:
- The planned site of intervention is totally occluded or has an anatomic configuration likely to prohibit adequate dilatation, and/or passage or implantation of the investigational device.
- Subject has multiple ipsilateral lesions of the target renal artery that cannot be covered by a single stent.
- There is a previously implanted stent in the target vessel or there is a previously implanted stent in the contralateral vessel < one year.
- Subject has fibromuscular dysplasia, in renal artery and/or other vascular bed.
- The target lesion site is associated with a thrombus.
- Target lesion treated with laser atherectomy, directional atherectomy or other adjuncts to percutaneous balloon angioplasty (PTA).
- Subject has a critical stenotic (> 70%) small accessory renal artery.
- Subject has an abdominal aortic aneurysm > 4.0cm in diameter or a severe atherosclerotic aorta.
- Main renal artery length ≤ 15mm precluding the safe deployment of a covered renal stent.
- Any lesion that would include blocking of renal artery side branch.
- Renal artery stenosis due to dissection of renal artery: spontaneous or traumatic.
Trial locations and contacts
12 sites in 1 country.
12 sites in 1 country
United States12 sites
Massachusetts General Hospital
Boston, Massachusetts, 02114
Mid Carolina Cardiology
Charlotte, North Carolina, 28204
Clearwater Cardiovascular and Interventional Consultants
Clearwater, Florida, 33756
OhioHealth Research Institute
Columbus, Ohio, 43214
Mission Cardiovascular Research Institute
Fremont, California, 94538
Wellmont CVA Heart Institute
Kingsport, Tennessee, 37660
Tennova Healthcare - Turkey Creek Medical Center
Knoxville, Tennessee, 37934
Medical Center of the Rockies
Loveland, Colorado, 80538
Advocate Health and Hospitals Corporation
Naperville, Illinois, 60563
NC Heart and Vascular Research
Raleigh, North Carolina, 27610
Beaumont Health Systems
Royal Oak, Michigan, 48073
Holy Name Medical Center
Teaneck, New Jersey, 07666
About this study
Official title: ARTISAN: iCAST™ RX De Novo Stent Placement for the Treatment of Atherosclerotic Renal Artery Stenosis in Patients With Resistant Hypertension
The purpose of this trial is to test how well the iCAST™ RX Stent works in patients diagnosed with atherosclerotic renal artery stenosis and whether or not increased blood flow by the stent will help to control blood pressure.
Read the detailed description
This is a prospective, single-arm, multicenter clinical trial that will take place at up to 25 US/ Outside US (OUS) sites. Primary endpoints have been determined to show the safety, effectiveness, and clinical outcomes of the iCAST™ RX Stent System. Safety and effectiveness will be evaluated based on the primary patency rate at 9-months on a per lesion basis evaluated against a performance goal of published studies with bare-metal stents. The primary clinical endpoint will assess the improvement in Systolic Blood Pressure (SBP) at 9-months as compared to baseline Systolic Blood Pressure.
Eligible subjects will undergo a two-week Medical Documentation Screening period to confirm resistant hypertension (SBP ≥ 155mmHg) while on maximum tolerable doses of ≥ three anti-hypertensive medications from at least three distinct classes of drugs, one of which must be a diuretic.
There must be documented clinical evidence to support likelihood of angiographic findings > 80% whether it is Duplex Ultrasound (DUS), Computed Tomography angiogram (CTa), Magnetic Resonance angiogram (MRa) or other medical evidence. After meeting screening and clinical eligibility criteria, subjects will undergo a baseline assessment for angiographic eligibility. After angiographic documentation of a ≥ 80% renal artery stenosis or Fraction Flow Reserve (FFR) < 0.8 is confirmed, the subject may be enrolled in the trial by placement of the investigational device.
The 9-month visit will include a follow-up DUS of the target renal artery. If the DUS is non-diagnostic due to an imaging problem, such as overlying bowel gas or body habitus, a second DUS may be attempted. If the DUS is indicative of ≥ 60% stenosis as determined by the core laboratory, or the second DUS remains non-diagnostic, a contrast angiogram will be used to assess the degree of restenosis of the covered stent(s).
Clinical follow-up visits will be required for all enrolled subjects at 30-days, 9-months, 12-months, 24-months, and 36-months. A 6-month and 18-month visit will occur via telephone to collect medication usage and Adverse Events (AEs) only. The 36-month clinic office visit will be required as the final safety visit.
- Conditions
- Renal Artery Stenosis, Hypertension, Renovascular
- Being tested
- iCAST™ Rx Stent System
- Keywords
- Renal Artery Stenosis, Renal Artery Obstruction, Renovascular Hypertension, Resistant Hypertension, Renal Revascularization, Atherosclerotic Renal Artery Stenosis, Atherosclerotic Renal Artery Stenosis (ARAS), Renal Artery Stenosis (RAS), Uncontrolled hypertension, Hypertension, Systolic blood pressure, Blood pressure
- Medical subject headings
- Renal Artery Obstruction, Hypertension, Renovascular, Hypertension
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
iCAST™ Rx Stent SystemDevice
Also called iCAST™ RX
All enrolled subjects will undergo primary stenting of the target lesion(s) by placement of the iCAST™ RX Stent System.
| Study group | Role | What they receive |
|---|---|---|
| iCAST RX™ Stent Systen | Experimental | All enrolled subjects will receive the iCAST RX™ Stent System Receives: Device: iCAST™ Rx Stent System |
What is being measured
The primary outcome is the main question the study is designed to answer.
Primary Patency
Primary patency rate at 9 months was defined as continuous patency without the occurrence of a total occlusion of the original lesion, without a re-intervention to treat a partial or total occlusion of the stented segment, or bypass of the stented segment due to clinically-driven restenosis or occlusion.
Measured: 9 months
Systolic Blood Pressure
Change in systolic blood pressure (SBP) at 9 months as compared to baseline SBP.
Measured: Baseline and 9 months
Secondary outcomes (11)
Procedure-Related Major Adverse Events (MAE)
The occurence of procedure-related MAEs is reported as a percentage of subjects with MAE. Inclusive of:
- Procedure- or device-related occurrence of death
- Q-Wave myocardial infarction (MI)
- Clinically driven target lesion revascularization (TLR)
- Significant embolic events defined as unanticipated kidney/bowel infarct, clinically driven by symptoms of abdominal or back pain and confirmed with CT scan or open surgery; lower extremity ulceration or gangrene; or kidney failure.
Measured: 30 days, 9 months
Technical Success
Technical success is defined as successful delivery and deployment of the iCAST™ RX Stent System with ≤ 30% residual angiographic stenosis after covered stent deployment (including post-dilatation) assessed via quantitative vascular analysis (QVA) by an independent core laboratory.
Measured: Day of Procedure
Acute Procedural Success
Acute procedural success is defined as technical success without the occurrence of MAE prior to hospital discharge.
Measured: Day of Procedure, prior to hospital discharge
Target Lesion Revascularization (TLR)
Target Lesion Revascularization (TLR) is measured as the proportion of subjects-lesions that require a clinically-driven reintervention of the target lesion through 9 months.
- A clinically-driven TLR is defined as a TLR (percutaneous balloon angioplasty (PTA), bare metal stent or repeat covered stent deployment, or surgical bypass) due to documented recurrent hypertension from 30-days post-procedure level and/or deterioration in renal function from baseline value, associated with angiographic core laboratory adjudication of a ≥ 60% diameter covered stent restenosis.
Measured: 9 months
Rate of Incidental TLR
The rate of incidental TLR is the rate of TLRs not meeting the definition of a clinically-driven TLR.
Measured: 9 months
Systolic Blood Pressure (SBP) Control
The change in SBP from baseline to 30 days
Measured: Baseline and 30 days
SBP Control
The change in SBP from baseline to 9 months
Measured: Baseline and 9 months
Secondary Patency Rate
Secondary patency rate at 9 months after a clinically-driven TLR which restores patency after total occlusion.
Measured: 9 months
Change in Number of Anti-Hypertensive Medications
Change in number of anti-hypertensive medications as compared to baseline.
Measured: Baseline and 9 months
Change in Renal Function
Renal function compared to baseline as measured by estimated Glomerular Filtration Rate (eGFR) at 30 days.
Measured: Baseline and 30 days
Change in Renal Function
Renal function compared to baseline as measured by estimated Glomerular Filtration Rate (eGFR) at 9 months.
Measured: Baseline and 9 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Aug 2012 (estimated)
- Study start23 Oct 2012
- Primary completion27 Jun 2018
- Study completion26 Oct 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Renal Artery StenosisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 68 participants (actual)
Sponsor and investigators
- Lead sponsor
- Atrium Medical Corporation
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Ken Rosenfield, MD, Principal investigator, Massachusetts General HospitalGary Ansel, MD, Principal investigator, OhioHealth Research Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01673373
- Sponsor's protocol ID
- iCAST™ RX-ARAS-001
- Acronym
- ARTISAN
- Status last verified
- Nov 2020
- First submitted
- 23 Aug 2012
- Last updated
- 20 Nov 2020
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Nov 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- ARTISAN: iCAST™ RX De Novo Stent Placement for the Treatment of Atherosclerotic Renal Artery Stenosis in Patients With Resistant Hypertension
- ClinicalTrials.gov ID
- NCT01673373
- Acronym / sponsor ID
- ARTISAN / iCAST™ RX-ARAS-001
- Conditions
- Renal Artery Stenosis, Hypertension, Renovascular
- Keywords
- Renal Artery Stenosis, Renal Artery Obstruction, Renovascular Hypertension, Resistant Hypertension, Renal Revascularization, Atherosclerotic Renal Artery Stenosis, Atherosclerotic Renal Artery Stenosis (ARAS), Renal Artery Stenosis (RAS)
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 68 participants (actual)
- Lead sponsor
- Atrium Medical CorporationIndustry (pharma, biotech, devices)
- Study start
- 23 Oct 2012 (actual)
- Primary completion
- 27 Jun 2018 (actual)
- Study completion
- 26 Oct 2020 (actual)
- First posted
- 28 Aug 2012 (estimated)
- Results
- Posted 13 Aug 2019
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this trial is to test how well the iCAST™ RX Stent works in patients diagnosed with atherosclerotic renal artery stenosis and whether or not increased blood flow by the stent will help to control blood pressure.
Detailed description
This is a prospective, single-arm, multicenter clinical trial that will take place at up to 25 US/ Outside US (OUS) sites. Primary endpoints have been determined to show the safety, effectiveness, and clinical outcomes of the iCAST™ RX Stent System. Safety and effectiveness will be evaluated based on the primary patency rate at 9-months on a per lesion basis evaluated against a performance goal of published studies with bare-metal stents. The primary clinical endpoint will assess the improvement in Systolic Blood Pressure (SBP) at 9-months as compared to baseline Systolic Blood Pressure.
Eligible subjects will undergo a two-week Medical Documentation Screening period to confirm resistant hypertension (SBP ≥ 155mmHg) while on maximum tolerable doses of ≥ three anti-hypertensive medications from at least three distinct classes of drugs, one of which must be a diuretic.
There must be documented clinical evidence to support likelihood of angiographic findings > 80% whether it is Duplex Ultrasound (DUS), Computed Tomography angiogram (CTa), Magnetic Resonance angiogram (MRa) or other medical evidence. After meeting screening and clinical eligibility criteria, subjects will undergo a baseline assessment for angiographic eligibility. After angiographic documentation of a ≥ 80% renal artery stenosis or Fraction Flow Reserve (FFR) < 0.8 is confirmed, the subject may be enrolled in the trial by placement of the investigational device.
The 9-month visit will include a follow-up DUS of the target renal artery. If the DUS is non-diagnostic due to an imaging problem, such as overlying bowel gas or body habitus, a second DUS may be attempted. If the DUS is indicative of ≥ 60% stenosis as determined by the core laboratory, or the second DUS remains non-diagnostic, a contrast angiogram will be used to assess the degree of restenosis of the covered stent(s).
Clinical follow-up visits will be required for all enrolled subjects at 30-days, 9-months, 12-months, 24-months, and 36-months. A 6-month and 18-month visit will occur via telephone to collect medication usage and Adverse Events (AEs) only. The 36-month clinic office visit will be required as the final safety visit.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| iCAST RX™ Stent Systen | Experimental | Device: iCAST™ Rx Stent SystemAll enrolled subjects will receive the iCAST RX™ Stent System |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| iCAST™ Rx Stent SystemAlso: iCAST™ RXAll enrolled subjects will undergo primary stenting of the target lesion(s) by placement of the iCAST™ RX Stent System. | Device | iCAST RX™ Stent Systen |
Primary outcome
Primary Patency
Time frame: 9 months
Primary patency rate at 9 months was defined as continuous patency without the occurrence of a total occlusion of the original lesion, without a re-intervention to treat a partial or total occlusion of the stented segment, or bypass of the stented segment due to clinically-driven restenosis or occlusion.
Systolic Blood Pressure
Time frame: Baseline and 9 months
Change in systolic blood pressure (SBP) at 9 months as compared to baseline SBP.
11 secondary outcomes
Procedure-Related Major Adverse Events (MAE)
Time frame: 30 days, 9 months
Technical Success
Time frame: Day of Procedure
Acute Procedural Success
Time frame: Day of Procedure, prior to hospital discharge
Target Lesion Revascularization (TLR)
Time frame: 9 months
Rate of Incidental TLR
Time frame: 9 months
Systolic Blood Pressure (SBP) Control
Time frame: Baseline and 30 days
SBP Control
Time frame: Baseline and 9 months
Secondary Patency Rate
Time frame: 9 months
Change in Number of Anti-Hypertensive Medications
Time frame: Baseline and 9 months
Change in Renal Function
Time frame: Baseline and 30 days
Change in Renal Function
Time frame: Baseline and 9 months
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Nov 2020.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Ken Rosenfield, MD principal investigator
Massachusetts General Hospital
Gary Ansel, MD principal investigator
OhioHealth Research Institute
12 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing iCAST™ Rx Stent System in people with Renal Artery Stenosis and Hypertension, Renovascular, run by Atrium Medical Corporation at 12 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 20 Nov 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 12 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Yes. Results are posted in the registry (first posted 13 Aug 2019). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Primary Patency (time frame: 9 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Nov 2020.