SBIR-STTR Award

An innovative ablation device for treating atrial fibrillation
Award last edited on: 12/28/2023

Sponsored Program
SBIR
Awarding Agency
NSF
Total Award Amount
$1,210,044
Award Phase
2
Solicitation Topic Code
BC
Principal Investigator
Amr Salahieh

Company Information

Apama Medical Inc

745 Camden Avenue Suite A
Campbell, CA 95008
   (408) 903-4094
   info@apamamedical.com
   www.apamamedical.com
Location: Single
Congr. District: 18
County: Santa Clara

Phase I

Contract Number: 1013560
Start Date: 7/1/2010    Completed: 12/31/2010
Phase I year
2010
Phase I Amount
$150,000
This Small Business Innovative Research (SBIR) Phase I Project will develop a novel balloon-based radio freqyency (RF) ablation catheter for atrial fibrillation treatment. Atrial fibrillation is the most common heart rhythm disturbance encountered in clinical medicine, accounting for 1/3 of hospital admissions for cardiac rhythm disturbances. Atrial fibrillation is frequently treated with catheter-based ablation; however, established RF methods are done via point to point manipulation using single electrode tip catheters. As a result, this technique is complex and time-consuming, requiring highly skilled physicians. Newer approaches include multi-electrode RF catheters, which have shown to create undesirable clot formations. Furthermore, mapping of the electrical activity in target tissues often requires the placement of multiple catheters in the left atrium, use of a 3D-mapping, and/or steering system. Current technologies have failed to overcome these limitations or have limited efficacy and/or safety. This project will develop a novel device that avoids these problems with an ablation balloon catheter that combines the conformability advantage of balloon-based approaches with simplicity and versatility of multi-electrode approaches. The device's utility will be validated in animal trials. This broader/commercial impact of this project, if successful, will be to generate a novel device that enables a safer, simpler and faster treatment for atrial fibrillation. This will allow a larger number of physicians to perform this procedure. The ease of use combined with lower cost (no need for expensive robotic and mapping systems) will fit well with the requirements of smaller hospitals that currently refer their patients to larger centers, as well as the more cost-efficient larger hospitals. This would be a major benefit to the 2.6 million atrial fibrillation patients in the U.S. alone that may be treated with catheter-based ablation. Atrial fibrillation is directly related to significant morbidity including debilitating palpitations, heart failure, recurrent hospitalizations, and stroke. An improved method of treating this condition will help mitigate these problems and treat a larger population of patients than possible with current methods and technology. As this device is a significant improvement over existing devices it is well-positioned to capture a large portion of the catheter ablation market

Phase II

Contract Number: 1127549
Start Date: 9/15/2011    Completed: 1/31/2016
Phase II year
2011
(last award dollars: 2015)
Phase II Amount
$1,060,044

This Small Business Innovation Research Phase II project proposes to develop a novel ablation balloon catheter to perform radiofrequency ablation on atrial fibrillation patients. The intellectual merit of this project is in its use of an innovative approach to positioning, mapping, and ablation for atrial fibrillation patients, negating the need for excessive catheter rotations and/or serial point ablations. This new technology significantly reduces user variability, procedural time, and the resultant cost burden on the hospital, physician, insurance payer, and patient. The research objectives for this project are to design and develop an improved prototype that enables verification of balloon-to-tissue contact; design and develop a 2nd generation radiofrequency generator capable of powering 20 electrodes; refine catheter design to increase reliability/robustness and sheathing capability; and develop 2nd generation handle that allows for the balloon extension. All of these changes will be validated through in vitro and in vivo testing. The broader impact/commercial potential of this project is an improvement in the treatment of atrial fibrillation, which is the most common heart rhythm disturbance encountered in clinical medicine, accounting for 1/3 of hospital admissions for cardiac rhythm disturbances. It is estimated that nearly 2.6 million individuals are currently afflicted with atrial fibrillation in the United States, with a projected increase to nearly 4.4 million people by the year 2030. Given the significant public health and economic impact of atrial fibrillation, there is an urgent need for practical and cost-effective approaches to treat atrial fibrillation. This technology aims to answer this need, providing an improved method of treatment for patients as well as highly-marketable technology that will save hospitals time and costs burdens