Sirolimus Coated Angioplasty Versus Plain Balloon Angioplasty

NCT ID: NCT04409912

Last Updated: 2021-08-06

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 170 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-11
• Study Completion Date: 2024-10-31

Brief Summary

A functioning dialysis access is critical to the delivery of hemodialysis therapy in patients with End Stage Renal Disease. Stenosis secondary to neo-intimal hyperplasia frequently occur within the dialysis access, resulting in dysfunction. Conventional balloon angioplasty is the current standard of care for treatment of stenosis but is associated with high rate of recurrence. Paclitaxel coated balloon has been shown to be superior to conventional balloon angioplasty in dialysis access interventions but recent meta-analysis has shown an increase in mortality when paclitaxel coated balloon and stents are used in lower limb angioplasty. Sirolimus coated angioplasty balloon are second generation drug coated balloon that have been shown to be effective in coronary artery interventions. Sirolimus is cytostatic in nature with good safety profile. In our pilot study, sirolimus coated balloon has been shown to be safe and effective in the salvaged of thrombosed arteriovenous graft. Therefore, the investigators are conducting a double-blinded, multi-center randomised control trial to compare the 6 month patency of arteriovenous fistula after intervention with sirolimus coated balloon versus conventional balloon angioplasty.

The investigators hypothesise that the addition of SCB after successful balloon angioplasty with conventional plain balloon is superior to conventional plain balloon angioplasty alone with decreased restenosis of the treated lesion, improved access circuit and treated lesion patency, and decreased number of interventions needed to maintain patency.

Detailed Description

Dialysis vascular accesses such as Arteriovenous Fistula (AVF) and Arteriovenous Grafts (AVG) are surgically created vasculatures used for hemodialysis in patients with End-Stage Renal Disease (ESRD). A functioning dialysis vascular access is critical to the delivery of life-saving hemodialysis (HD) treatment to these patients. Unfortunately, neointimal hyperplasia frequently occurs within the dialysis vascular access, resulting in stenosis, poor flow and thrombosis with loss of function. The durability of both AVF and AVG are poor, with an almost 50% failure rate after a median lifetime of 3 to 7 years for AVF and 12 to 18 months for AVG. Vascular access failure is the most common reason for hospitalization among HD patients. The global healthcare costs for treating vascular access-related complications amount to USD 18 billion, and in USD 1 billion in the US alone. These figures are set to increase, due to the increase in the prevalence of access interventions and hemodialysis patients globally. Singapore has one of the highest ESRD rates in the world and the investigators are facing an increasing number of patients with ESRD and the majority of the patients opting for hemodialysis as their treatment modality. As such, vascular access-related complication is set to be a major contribution of healthcare cost in our nation.

The current gold standard therapy for the treatment of stenosis in dialysis access is plain balloon angioplasty (BA). Despite its widespread availability and minimally invasive nature, the mid- and long-term patency with BA in patients with ESRD is poor. The reported average primary patency after BA is around 40-50% at 1 year. Multiple repeated angioplasty is required to maintain the patency of the vascular access. Hence, there is an urgent clinical need to improve the patency of dialysis vascular access.

Recently, the use of stents, in particular stent graft, has been shown to be superior to angioplasty for stenosis occurring at the site of venous anastomoses of an AVG. The incidence of patency of the treatment area was significantly greater in the stent-graft group than in the balloon-angioplasty group (51% vs. 23%, P<0.001), as was the incidence of patency of the access circuit (38% vs. 20%, P=0.008) at 6 months. For cephalic arch stenosis in AVF, the use of stent graft has also been shown to be superior to bare metal stent. The 6 month primary patency for stent graft and bare stent was 81.8 and 39.1%, respectively. One-year primary patency for stent graft and bare stent was 31.8 and 0.00%, respectively (P = 0.002). However, the use of stent graft for the management of dialysis vascular access is not without any concern. In particular, re-stenosis can occur within the stented segment (post stent 12-month primary patency is 46%), resulting in the need for repeat angioplasty. Future stent deployment in the re-stenotic segment may also not be feasible due to the presence of the stent. Moreover, the presence of a stent can impede future surgical revision or new access creation within the same vessel.

Paclitaxel-coated balloon angioplasty (PCBA) has also been shown recently to be superior to plain BA in the treatment of stenosis in dialysis vascular access. This is because the very intervention used to treat the underlying stenosis by plain BA can induce vascular injury and accelerate intimal hyperplasia, resulting in rapid restenosis and the need for repeated procedures to maintain vessel patency. By releasing Paclitaxel, which is an anti-proliferative drug, locally into the vessel wall during balloon contact, it will blunt the acceleration of intimal hyperplasia response, resulting in improved primary patency after angioplasty. Additionally, unlike stents, PCBA does not leave a permanent structure that may impede future surgical revision. In a small 40 patient pilot study, the primary unassisted patency in the PCBA group was significantly better than the plain BA group at 6 (70 % versus 25 %) and 12 months (35 % versus 5 %, p <0.001) respectively. Recent randomized control trials have also shown the superiority of PCBA over plain balloon angioplasty in the treatment of stenosis in dialysis vascular access. However, concerns had also arisen recently in the use of PCBA. In large lower limb studies involving the use of PCBA, meta-analysis had revealed an increased risk of death in patients that are treated with PCBA or paclitaxel-coated stent. This had led to warning from the United States Food and Drug Administration (FDA) and the issue of guidelines from the interventional societies

Sirolimus coated balloon (SCB) is the new generation of drug-eluting balloons available in the market. Compared to Paclitaxel, sirolimus is cytostatic in its mode of action with a high margin of safety. It has a high transfer rate to the vessel wall and effectively inhibits neointimal hyperplasia in the porcine coronary model. In the coronary artery interventions, preliminary clinical studies using SCB have also shown excellent procedural and 6-month patency.

The effectiveness of SCB in patients with dialysis access dysfunction has been shown in a small pilot study in the salvage of thrombosed AVG and investigators postulate that SCB will be a viable option in patients who requires treatment with drug-coated balloon.

The investigators aim to conduct a multicenter double-blinded randomized controlled trial to compare the 6 month unassisted patency rate of SCB angioplasty versus plain balloon angioplasty in the management of stenosis in arteriovenous fistula.

RECRUITMENT:

Patients with matured AVF (in use for more than 1 month) that are dysfunctional and are already scheduled to undergo balloon angioplasty will be considered for the trial. Patients will be consented if they fulfill the preliminary eligibility criteria and are agreeable to participate in the study. Once all the eligibility criteria are fulfilled, including angiographic criteria assessed on the day of the procedure, the patient is entered into the trial and randomised. Patients who are unsuitable for the trial will be treated in the conventional way with PB and considered as screen failure.

STUDY PROCEDURE:

The AVF will be assessed with ultrasound for possible access sites. All patients will undergo a fistulogram which is obtained by injection of contrast. The access site will be left to the discretion of the procedurist. The fistulogram should include the entire dialysis circuit from the arteriovenous anastomosis to the central veins. The suggested approach would include a fistulogram via an 18 Gauge cannula inserted into the arterialised vein. When there is no spontaneous reflux of contrast into the artery, reflux opacification of the arteriovenous (AV) anastomosis is achieved by injecting contrast during inflation of a blood pressure cuff or a tourniquet around the arm. Alternatively, a trans-radial or arterial approach may be used to obtain the fistulogram

Based on fistulogram findings, the access site will be placed up to the discretion of the procedurist. If an 18G cannula is used, it may be exchanged for a vascular sheath that is sized appropriately based on the planned balloon sizes). Alternatively, the 18G cannula may be removed and a new access site for intervention may be chosen. A new puncture will be performed with the insertion of a vascular sheath (sized appropriately according to planned balloon sizes). Two access sites (both antegrade and retrograde) may be needed in certain cases. A trans-radial or arterial approach may also be considered if necessary

In the event that opacification of the anastomosis was not earlier achieved even with inflation of a blood pressure cuff around the arm, it will be performed via contrast injection through a catheter in the feeding artery.

When there is more than 1 stenosis, all the lesions will be labelled and treated with conventional balloon angioplasty (from the AV anastomosis up to, but not including, the subclavian vein). Lesions are considered separate if they are separated by a gap of at least 2 cm. The lesion or lesions will be dilated with standard angioplasty that is sized similar to the adjacent reference vessel. Inflation time will be at least 1 minute per inflation. The balloon will be inflated to an appropriate inflation pressure as per institution standardised practice to achieve <30% residual stenosis and satisfactory thrill. If there is significant residual stenosis after angioplasty (defined as > 30% stenosis), repeat angioplasty with the same standard angioplasty balloon or a larger standard angioplasty balloon may be used at operator's discretion. High-pressure angioplasty balloon or cutting balloon may also be used, if necessary, in the event of resistant stenosis. In stenotic segment adjacent to aneurysmal segment, where the percentage of stenosis is difficult to determine, the treated segment should reach at least reach 6mm.

Randomisation occurs when all the lesions are treated adequately, defined as less than 30% residual stenosis after standard treatment.

Patients will be randomised to receive either the sirolimus coated balloon or plain balloon. Repeated angioplasty of the stenotic segments that were successfully treated (defined as less than 30% residual stenosis) will be performed using sirolimus coated balloon (for patient randomised into the sirolimus balloon arm) or plain/placebo balloon (for patients randomised into the placebo arm)

POST-PROCEDURE ULTRASOUND SCAN:

All participants will receive an ultrasound scan of their AVF after their procedure before discharge. The diameter of the vessel at the treated sites will be measured and documented. Brachial artery flow and flow within the outflow vein will also be measured and documented

• Patency definitions are defined based on SIR reporting standards (Gray et al., 2003):

Post-intervention target lesion patency:

Interval after intervention until the next re-intervention at or adjacent to the original treatment site or until the access is abandoned. Percutaneous or surgical treatments of a new arterial or venous outflow stenosis/occlusion (including access thrombosis) that do not involve or exclude the original lesion from the access circuit are compatible with lesion patency. The creation of new access that incorporates the target lesion into the new access circuit is also compatible with target lesion patency.

Post-intervention access circuit primary patency:

Interval following intervention until the next access thrombosis or repeated intervention. It ends with the treatment of a lesion anywhere within the access circuit, from the arterial inflow to the superior vena cava-right atrial junction.

Post-intervention access circuit assisted primary patency:

Interval after intervention until access thrombosis or surgical intervention that excludes the treated lesion from the access circuit. Percutaneous treatments of either restenosis/occlusion of the previously treated lesion or a new arterial or venous outflow stenosis/occlusion (excluding access thrombosis) are compatible with assisted primary patency.

Post-intervention access circuit secondary patency:

Interval after intervention until the access is surgically declotted, revised or abandoned. Thrombolysis and percutaneous thrombectomy are compatible with secondary patency.

^Complications will be categorised according to SIR definitions of minor or major complications (Aruny et al., 2003):

A major complication is defined as one that:

1. require therapy, minor hospitalisation (< 48 hours),

2. require major therapy, unplanned increase in the level of care, prolonged hospitalisation (>48 hours),

3. leads to permanent adverse sequelae, or

4. death

A minor complication is one that:

1. requires no therapy with no consequence,

2. requires nominal therapy with no consequence; includes overnight admission for observation only.

POST-PROCEDURE FOLLOW-UP ULTRASOUND SCAN OF AVF:

Patients will be followed-up at:

3 months (± 1 weeks): assessment of primary outcome 6 months (± 4 weeks): assess the target lesion and access circuit. 12 months (± 4 weeks): assess AVF patency and study closure

Conditions

End Stage Renal Failure on Dialysis; Arteriovenous Graft Occlusion

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Sirolimus coated balloon

The trial product is MagicTouch sirolimus drug coated balloon (Concept Medical). Sirolimus will be transferred from the balloon to the vessel wall by inflating the sirolimus coated balloons at 2 minutes at rated burst pressure (typically 12 to 14ATM). All the lesions within the dialysis circuit with sirolimus coated balloon.

Group Type: EXPERIMENTAL

Sirolimus coated balloon

Intervention Type: DEVICE

Sirolimus has a high transfer rate to the vessel wall and effectively inhibit neointimal hyperplasia in the porcine coronary model. In coronary artery interventions, preliminary clinical studies using sirolimus coated balloon have shown excellent procedural and 6 month patency. The effectiveness of sirolimus coated balloon in patients with dialysis access dysfunction has been shown in a small pilot study in the salvage of thrombosed arteriovenous graft.

When compared to Paclitaxel, sirolimus is cytostatic in its mode of action with a high margin of safety.

Plain balloon

The plain balloon or placebo will not be coated. The plain balloon will be inflated at 2 minutes at rated burst pressure (typically 12 to 14 ATM). Plain balloon will be applied to all the narrowed segment of the dialysis circuit

Group Type: PLACEBO_COMPARATOR

Plain balloon

Intervention Type: DEVICE

Plain balloon angioplasty is the current standard therapy to treat stenosis in dialysis access. However, the mid and long term patency of plain balloon angioplasty in patients with end stage renal disease is poor. The average primary patency is around 40 to 50 percent at 1 year and multiple repeated angioplasty is required to maintain the patency of the vascular access.

Interventions

Sirolimus coated balloon

Sirolimus has a high transfer rate to the vessel wall and effectively inhibit neointimal hyperplasia in the porcine coronary model. In coronary artery interventions, preliminary clinical studies using sirolimus coated balloon have shown excellent procedural and 6 month patency. The effectiveness of sirolimus coated balloon in patients with dialysis access dysfunction has been shown in a small pilot study in the salvage of thrombosed arteriovenous graft.

When compared to Paclitaxel, sirolimus is cytostatic in its mode of action with a high margin of safety.

Intervention Type: DEVICE

Plain balloon

Plain balloon angioplasty is the current standard therapy to treat stenosis in dialysis access. However, the mid and long term patency of plain balloon angioplasty in patients with end stage renal disease is poor. The average primary patency is around 40 to 50 percent at 1 year and multiple repeated angioplasty is required to maintain the patency of the vascular access.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Age 21 to 85 years

2. Patient who requires balloon angioplasty for dysfunction arteriovenous fistula

3. Matured AVF, defined as being in use for at least 1 month prior to angioplasty

4. 4. Successful angioplasty of the underlying stenosis, defined as less than 30% residual stenosis on Digital Subtraction Angiography (DSA) based on visual assessment of the operator and restoration of thrill in the AVF on clinical examination. (For concurrent asymptomatic or angiographically not significant central vein stenosis, patients can be included if no treatment is required.)

Exclusion Criteria

1. Patient unable to provide informed consent

2. Thrombosed or partially thrombosed AVF

3. Presence of symptomatic or angiographically significant central vein stenosis who require treatment, with more than 30% residual stenosis post angioplasty

4. Patients who had underwent stent placement within the AVF circuit

5. Patient who are currently enrolled in other drug eluting balloon trials

6. Sepsis or active infection

7. Recent intracranial bleed or gastrointestinal bleed within the past 12 months

8. Allergy to iodinated contrast media, anti-platelet drugs, heparin or sirolimus

9. Pregnancy

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National University Hospital, Singapore

OTHER

Sponsor Role: collaborator

Sengkang General Hospital

OTHER

Sponsor Role: collaborator

Singapore General Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Chieh Suai Tan, MD

Role: PRINCIPAL_INVESTIGATOR

Singapore General Hospital

Locations

National University Hospital

Singapore, , Singapore

Site Status: RECRUITING

Singapore General Hospital

Singapore, , Singapore

Site Status: RECRUITING

Sengkang General Hospital

Singapore, , Singapore

Site Status: RECRUITING

Countries

Singapore

Central Contacts

Chieh Suai Tan, MD

Role: CONTACT

tan.chieh.suai@singhealth.com.sg

+6581231127

Facility Contacts

Jackie Pei Ho, MD

Role: primary

surhp@nus.edu.sg

Chieh Suai Tan, MD

Role: primary

tan.chieh.suai@singhealth.com.sg

Edward Tieng Chek Choke, MD

Role: primary

edward.choke.t.c@singhealth.com.sg

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Other Identifiers

2019/2896

Identifier Type: -

Identifier Source: org_study_id