The amount of hassle and anxiety this will save me is impressive on its own, but so to is the ability to have a normal lifestyle (such as going out for a drink) without having to worry about whether or not I’m always in range of a hospital that I want to spend 3 days in if I’m unlucky
Thank you and good luck!
So, I think this is a great idea.
She is currently waiting for an ablation, which was a close call vs leaving her in it, but she wanted to try it.
Typically at my institution we load first and cardiovert later if needed. How is that handled in your system?
Also, what is the clinicaltrials.gov registration for your completed Phase I?
Phase I Software validation doesn't require clinicaltrials.gov registration, but our Phase II trial will be per FDA!
Also, I didn't realize that Phase I trials didn't have to be registered on clinicaltrials.gov! But you're right, they're specifically exempted[1].
1 = https://clinicaltrials.gov/ct2/manage-recs/fdaaa#WhichTrials...
Congratulations on the launch, and I wish you well, and hope it is of great use to thousands!
> existing FDA-cleared hardware Can you please link to this?
Or perhaps more to the point - the problem you mention in OP seems, as described, like it's already solved by Kardia, what was missing that you had to build?
Now, how do I also get your software that will work with this hardware?
> The 510(k) Clearance process is one of two ways by which a medical device manufacturer can obtain approval from the Food and Drug Administration, although legally, a device clearance under this section is not a true “approval.” 510(k) Clearance simply gives the company permission to market its product, based on comparison to a “predicate” [previously approved] device.[1]
Basically, If a somewhat similar device is already on the market, the FDA will clear the new device for the market.
[0] https://www.fda.gov/medical-devices/device-approvals-denials...
- What makes you "better" than your competitors, perhaps especially those of your competitors with substantially deeper pockets than you ? (e.g. Apple Watch which also has "ECG" functionality).
- Building on the above, how's the prior art looking on the patents ?
- Finally, general cynicism on "home ECG".... clinical evaluation is 12 lead ECG. Can you really get away with substantially less input ? (Garbage In - Garbage Out).
There are single lead chest ECG patches used for specific diagnostic reasons. Zio patch is one common device used. [0]
If patent filings are a guide[1], Apple are aware and have been investigating options for user-friendly additional sensors elsewhere on the body.
Whether it comes to market is another matter, of course.
[1] http://patft1.uspto.gov/netacgi/nph-Parser?patentnumber=1108...
I hope your service makes ECG more accessible to identify heart diseases earlier.
Do you have a link to the study? Isn’t that a relatively low number of patients to validate against?
It seems fair to summarize this as a "smart(er) Holter monitor".
I wonder whether there exist some Holter monitors that could be made more functional with just a firmware reprogramming job. You really need interfacing though: BT, Wi-Fi, ...
I am genuinely curious to see the breakdown of where that money goes
On the outpatient facility they would have charged $1100.
On a related note, I've been thinking about building something similar for personal use using one of those audrino based ECGs (just recording and then finding anomalies). Never got the time though.
I've already validated that the idea would be useful. There's a potential annual patient population of around 7 million people in the US. Even at 10% adoption, that could be revenue of $100-200M with a conservative guesstimate profit margin of 10-20% at that level (variable costs are low, so that should be higher as it scales). Current price of testing is high enough that I think this device could fit into that range or under cut it, with a multifaceted improvement to patient experience. A brief search turned up no competitors.
Now I'm trying to decide if I should spend the money to build a prototype and file a provisional patent or not. It depends on exactly how expensive and lengthy the approval process is, how HIPPA might or might not apply, etc. The type of software it will require will also be a challenge for me since I've never made anything like this.
I also have an lvad and spend a lot of time in the hospital taking quite a few medications