What the registry aims to learn
The planned follow-up focuses on pain intensity, daily function and quality of life over approximately twelve months. Repeated questionnaires can help describe changes, patterns and experiences, but cannot, by themselves, establish that a treatment caused improvement.
Who may want information
Adults experiencing persistent back, neck, joint or nerve-related pain, peripheral neuropathy, headaches or similar chronic symptoms may ask about eligibility. A consultation is not an acceptance or enrollment decision.
How participation works
Patients make clinical decisions with their treating clinician independently of the registry. If enrollment is open and an individual qualifies, staff explain privacy protections, data collection, follow-up schedule, voluntariness and the appropriate informed-consent process.
- Initial inquiry and screening
- Separate clinical evaluation and treatment decisions
- Scheduled outcome surveys over twelve months
Costs and treatment choices
Clinical services are self-pay and are generally not covered by insurance. Participants may pay ordinary clinical fees; costs, alternatives and optional participation should be explained before any decision. Enrolling in a registry is not a condition of receiving medically appropriate care.
An essential regulatory boundary
The registry is not a clinical trial that assigns investigational products, and it does not authorize the use of unapproved exosomes, MSCs, MUSE cells or Wharton’s jelly. Any investigational administration must separately comply with applicable federal and state requirements. No clinical benefit is guaranteed.
Current registry status
The clinic is developing and communicating information about its observational program. Please contact the office for the current protocol, ethics review, enrollment status and eligibility criteria; this website does not claim that an IRB has approved enrollment.