Because we are dealing with human subjects, the data obtained is incredibly sensitive. We need to ensure we get patient consent to test this device, and can do so by asking them to sign a consent waiver and discussing the potential dangers of testing this untested device. The data that we collect from these tests must also be treated confidentially and ethically, as they will likely contain sensitive information.
Parts List
Tools List
With this project, Lori should be able to continue her study using the data from our modified catheter. We tried to simplify the catheter assembly as much as possible, though it does take some practice to do efficiently. Furthermore, one of our goals with this design was to create a reusable system, but the EndoFLIP catheters have a usage limit. The next step would be to move away from EndoFLIP and make an entirely original balloon catheter with a better and more customizable interface.
Overall, our design is a better alternative to existing solutions. Although length-tension manometry and anal sphincter electromyography are more affordable due to reusability, the modified EndoFLIP catheter is more comfortable and gives more accurate and detailed data. With this modification, we hope that more studies can be performed to help women suffering from pelvic floor disorder.
Editor: Juhi Madan