Silk Road Medical First in Man Study - Neuroprotection During Carotid Stenting and Angioplasty — PROOF  

Carotid Artery Diseases Clinical Trial

Official title: SILK ROAD™ MEDICAL EMBOLIC PROTECTION SYSTEM: FIRST IN MAN STUDY "The PROOF Study"

Status Completed

Clinical Trial Summary

Cerebral embolization during carotid artery stenting (CAS) can often precipitate severe adverse neurological effects. Most major clinical studies of CAS have used distal filters for cerebral protection and have compared the neurologic complication rates with those of carotid endarterectomy (CEA). Many currently available embolic protection devices, however, have limited efficacy in capturing microembolic debris that is liberated during stenting, pre-dilatation and post-dilatation. Distal protection systems are furthermore limited by the need to cross the lesion prior to deployment. Some studies have shown a relatively high incidence of cerebral infarction even when distal protection devices are employed.

Cerebral protection with carotid flow reversal is a method that was developed by Parodi, et al., as an alternative to the use of distal protection devices. While novel in its approach, this method too has its limitations. Criado, et al., developed a derivative technique that employs carotid flow reversal prior to traversing the stenosis and can be accomplished by directly accessing carotid anatomy without the use of the transfemoral approach. Major benefits to this method include the ability to perform the procedure on patients with severe carotid tortuosity and difficult aortic arch anatomy.

Clinical Trial Description

Carotid artery disease is known to increase the risk of neurologic consequences such as transient ischemic attacks (TIA), ischemic stroke, or death due to the release of embolic particles in the vessels supplying the brain. Two principal treatments, carotid endarterectomy (CEA), and carotid artery stenting (CAS), are used to treat this disease. Embolic protection devices, both distal filters and occlusive devices, are employed during the CAS procedure to reduce the risk of carotid plaque embolus secondary to instrumentation during carotid intervention. Existing embolic protection devices are placed using a transfemoral approach and thus have potential for particle embolization while crossing the aortic arch, supraaortic trunk and the carotid lesion before cerebral protection is in place. Other limitations of these devices include the potential for carotid intimal injury, dissection or spasm during deployment, and release of emboli during retrieval.

Noting that carotid embolization remains the "Achilles heel" of carotid artery stenting, an alternative approach to embolic protection was developed by Juan Parodi. The system works by balloon occlusion of the common carotid artery and external carotid artery. An arteriovenous fistula is created with sheaths and catheters and provides retrograde (reverse) blood flow from the internal carotid artery (ICA) and the common carotid artery (CCA) to the femoral vein.

Embolic particles released during CAS pass retrograde through a catheter into a 180 micron filter before the blood re-enters the venous system. (Parodi, Ferreira et al. 2005) A variation of the reverse flow approach utilizing a surgical, transcervical approach to the carotid artery was developed to address challenges and risks associated with the placement and use of existing embolic protection devices. Criado et al. (2004) describe the use of flow reversal during CAS via a transcervical surgical cutdown, access and proximal occlusion of the CCA and establishment of a carotid artery - internal jugular (IJ) vein fistula. (Criado, Doblas et al. 2004).

A difference between the transfemoral-based Parodi approach and the transcervical-based Criado approach is the removal by Criado of the ECA occlusion step. In the Criado approach, the procedure is designed such that the flow is reversed in both the internal and the external carotid arteries, whereas in the Parodi procedure, flow reversal occurs only in the ICA. Another difference in the Criado system is the shorter length and larger diameter tubing afforded by the transcervical approach. The rate of flow reversal enabled by the Criado arteriovenous shunt is higher and is designed to overcome the potential for antegrade flow from the ECA to the ICA.

However, as reported by both Parodi and Criado, active aspiration is often utilized during critical periods of the procedure, to guarantee robust reversal of flow in the ICA.

Similarly in 2004, Chang, et al., reported the use of a direct transcervical approach through a 2cm incision at the base of the neck in 21 CAS patients with a 0% technical failure rate and a 0% thirty-day combined stroke or mortality rate. A similar approach of direct access to the low common carotid artery and the creation of a shunt to the internal jugular was used with carotid occlusion leading to a state of flow reversal. In some cases in this series, a balloon was placed in the external carotid artery. (Chang et al, 2004) Subsequently, Criado et al reported in the Journal of Vascular Surgery in 2004 on a series of fifty patients who underwent carotid artery stenting via this transcervical approach. Using the technique described above, flow was reversed in the ICA by occluding the CCA and establishing a carotid-jugular vein fistula. There was technical success in all 50 procedures and no strokes or deaths occurred. The procedure was tolerated by all but two (4%) of patients. Complications included major and minor carotid artery dissections, which resolved after stent placement. Two transient ischemic attacks (TIA) occurred, one in a patient in whom flow reversal was not successful, and one patient with a contralateral ICA occlusion who suffered a contralateral TIA.(Criado, Doblas et al. 2004).

Criado et al. further report in the Journal of Vascular Surgery in 2004 on a series of 10 awake patients undergoing transcervical carotid artery stenting with flow reversal. Procedural success was achieved in all 10 cases and flow reversal was well tolerated. Cerebral oxygenation during ICA flow reversal was comparable to that during CCA occlusion. ICA angioplasty balloon inflation produced a decrease in SVO2 significantly greater than that occurring during ICA flow reversal. (Criado, Doblas et al. 2004) Finally, Criado et al report on the perioperative and 3 year follow up results of 103 consecutive carotid artery stenting procedures done with a transcervical approach using carotid flow reversal for cerebral protection performed over a 28 month period in 97 patients. Technical success was achieved in 100 cases (97%). No major strokes or deaths occurred. Three awake patients (4%) did not tolerate flow reversal and complications included one ipsilateral TIA, one contralateral TIA, and two minor strokes. There were two wound complications and one major arterial complication. Mean flow reversal time was 21 minutes. At 40 months, the stent patency rate on an intention-to-treat basis was 95%, and the stroke-free survival was 91%. (Criado, Fontcuberta et al. 2007).

In 2006, Ribo and colleagues monitored transcranial doppler (TCD) as part of their standard carotid practice where 23 of 65 patients underwent transcervical carotid stenting using Criado's technique. Mean reversal time was about 15 minutes and well tolerated. TCD monitoring showed an absence of air/solid emboli during stent deployment and angioplasty confirming the presence of reverse flow. Baseline middle cerebral artery (MCA) flow by TCD of 47 cm/sec was substantially decreased with clamping of the common carotid (representing reversal of internal carotid flow). Initial mean antegrade MCA velocity of 30 cm/sec was present post clamping suggesting that there was adequate hemispheric blood flow to be clinically tolerated (Ribo et al. 2006).

Silk Road Medical has developed a system of sheaths, shunts and flow regulators, called the SRM Embolic Protection System, to apply the demonstrated benefits of the Criado and Chang approaches and improve further on ease of use and effectiveness. Silk Road Medical has provided an arteriovenous shunt with the ability to regulate from a low, baseline flow to a higher flow rate. This is accomplished by modulating the flow resistance of a shunt line which connects an arterial and a venous sheath. Because of potential patient intolerance to long periods of high reverse flow, the flow controller enables the user the set the shunt high flow only during periods of the procedure which are high risk for embolic debris (angiography, angioplasty, stent placement). This system eliminates the need for an active aspiration step, and theoretically enables the user to balance patient tolerance needs with optimal embolic protection.

The conclusion from the series of above literature is that transcervical CAS with carotid flow reversal can be accomplished with a high rate of technical success, a very low rate of major adverse events, and an excellent 3 year stroke free survival and stent patency rate. The purpose of this initial investigation is to determine if the SRM Embolic Protection System enables flow reversal of the carotid artery, is compatible with the techniques, devices and equipment used during a carotid artery stenting CAS procedure, and does not present any additional safety risks to the patient. ;

Related Conditions & MeSH terms

• Carotid Artery Diseases

• NCT number: NCT01264419
• Study type: Interventional
• Source: Silk Road Medical
• Status: Completed
• Phase: N/A
• Start date: March 2009
• Completion date: July 2012