Did they say what criteria the 10% meets? That would be helpful.Below is from the Brai3n clinic, one of the centers involved in the trial.
So, 6% of the population will find this effective.
Did they say what criteria the 10% meets? That would be helpful.Below is from the Brai3n clinic, one of the centers involved in the trial.
So, 6% of the population will find this effective.
Well, I believe Brai3n was part of the TENT-A3 trials, so you would think they know what they're talking about. However, after looking at the trial eligibility criteria, nothing really stands out that would suggest 90% of the tinnitus population wouldn't be eligible.
There's a user experiences thread with 50+ reports. Most people say it's trash.I developed tinnitus in October 2023 and have tried various treatments, but like most of you, I haven't had any success.
My question is about the Lenire device. Has anyone here actually tried it, and if so, has it provided any real help in reducing your tinnitus?
This device is quite expensive, and insurance doesn't cover it, so I'm curious to hear about any results from people who have used it.
Thanks for sharing your experience and warning others. I'm sorry to hear about your situation, but 57.7 percent? That's unbelievable! Their materials mention success rates in the high 80s!Tinnitus worse after using Lenire? Same here! I spent $4,500 on the device and audiology services, plus an additional $500 on travel. After completing the full 84-hour protocol, the volume and intensity of my tinnitus actually worsened.
When I reached out to the Lenire provider to request an adjustment, they encouraged me to try the treatment again. I did, after a four-month break, but only lasted two weeks because I couldn't tolerate it.
I then asked about their clinical data, and they informed me that for my "mild to moderate tinnitus," the success rate was 57.7%. When I pointed out that this information wasn't shared with me at the time of purchase (last December), they claimed the data was only recently updated.
I strongly believe that Lenire and its authorized audiology practices need to be much more transparent about the following:
Buyer beware!
- There is a significant risk that you may not see any improvement.
- There is no recourse if the treatment doesn't work for you.
- Lenire will not accept returned devices, even though they could refurbish them and sell them at a lower price.
Hey, could you tell me how you reached out to them? I know a different company took over to handle Lenire for Neuromod, but I've lost all contact information. Neuromod hasn't replied to my email, so I'm a little unsure how to reach them these days.Tinnitus worse after using Lenire? Same here! I spent $4,500 on the device and audiology services, plus an additional $500 on travel. After completing the full 84-hour protocol, the volume and intensity of my tinnitus actually worsened.
When I reached out to the Lenire provider to request an adjustment, they encouraged me to try the treatment again. I did, after a four-month break, but only lasted two weeks because I couldn't tolerate it.
I then asked about their clinical data, and they informed me that for my "mild to moderate tinnitus," the success rate was 57.7%. When I pointed out that this information wasn't shared with me at the time of purchase (last December), they claimed the data was only recently updated.
I strongly believe that Lenire and its authorized audiology practices need to be much more transparent about the following:
Buyer beware!
- There is a significant risk that you may not see any improvement.
- There is no recourse if the treatment doesn't work for you.
- Lenire will not accept returned devices, even though they could refurbish them and sell them at a lower price.
I'm sorry to hear about your experience with Lenire.I purchased my Lenire device in December 2023 from Gatwick Audiology. Prince, the audiologist, was very nice and believed I was a good candidate for Lenire.
My Tinnitus Handicap Score is 76, and my tinnitus is bilateral. I have only a very slight hearing loss in my left ear, which has been stable for years.
My tinnitus started immediately after my first COVID-19 shot, which I was eager to get because I am clinically vulnerable.
Initially, my tinnitus increased dramatically after using the device. Prince advised me to start slowly, using it for 10 minutes a day. I was hopeful that my strong reaction to the device indicated I would be receptive to the treatment.
I gradually increased my usage and have been using the device twice a day, consistently, since March. Unfortunately, there has been no improvement at all.
Prince discussed my case with Lenire, and they took the device back to ensure it was working properly. During the three weeks it was away, my tinnitus gradually worsened (something I didn't think was possible). Upon receiving the device back, it has returned to the level it was at before. My initial Tinnitus Handicap Score was 76, and when I retook it last week (on September 24), it was 70. There has been no significant improvement, and I feel like my savings have been wasted.