Patient Registry

Your Voice Matters. Your Data Drives the Research.

Every clinical trial starts with a patient registry. Every breakthrough begins with people willing to stand up and say: “I have tinnitus. I want a cure. And I'm ready to be part of the solution.”

1,247

Registry Members

Countries Represented

7.2 yrs

Avg Tinnitus Duration

312

Trial-Ready Volunteers

Why This Matters

Patient Registries Change Everything

A patient registry isn't just a mailing list. It's the scientific foundation that makes clinical trials possible.

Demonstrates Demand

When we approach IRBs, research partners, and funders, a large registry proves that real people are waiting for this research. Numbers speak louder than proposals.

Enables Trial Design

Registry data on severity distribution, duration, demographics, and comorbidities helps us design better, more targeted clinical trials — increasing the chance of meaningful results.

Fast Recruitment

When the pilot study launches, we need to enroll 20-30 participants quickly. A pre-screened, engaged registry means we can go from approval to enrollment in weeks, not months.

Join the Registry

Be Part of the Solution

Registering takes 2 minutes. Your data is protected and will only be used for research purposes.

First Name *

Last Name *

Email Address *

Age

How long have you experienced tinnitus? *

Severity Level *

I'm interested in participating in clinical trials

You'll be notified when trials open. No obligation — just early access to enrollment.

I am a military veteran

Veterans may qualify for priority enrollment in future studies.

I am a professional musician or audio professional

Helps us understand occupational tinnitus patterns.

Anything else you'd like us to know? (optional)

Your Privacy Matters

Your data is encrypted and stored securely. It will only be used for research purposes and will never be sold or shared with third parties. You can request deletion at any time. Registry participation does not obligate you to participate in any clinical trial.

After You Register

What Happens Next

Step 01

Confirmation

You'll receive a confirmation email with your registry ID and a welcome packet about the research program.

Step 02

Updates

Monthly emails with research progress, milestone updates, and community news. No spam, ever.

Step 03

Trial Notification

When clinical trials open for enrollment, you'll be among the first to know — with early access to apply.

Step 04

Community

Access to private forums, AMAs with researchers, and a community of people who understand what you're going through.

Every Name on This Registry Is a Voice Demanding Change

The more people who register, the louder the message: this condition deserves real research, real funding, and real answers. Don't wait for someone else to go first.