Idaho Falls, IDNCT07456865Now EnrollingIRB Ready

Urge Urinary Incontinence Clinical Trial in Idaho Falls, ID

Access cutting-edge urge urinary incontinence treatment through this clinical trial at a research site in Idaho Falls. Study-provided care at no cost to qualified participants.

Sponsored by MedtronicNeuro

Quick Self-Assessment

See if you qualify for this Idaho Falls location

Preparing your pre-screening questions…

Expert Care in Idaho Falls

Access urge urinary incontinence specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related urge urinary incontinence treatment provided free

Apply for This Idaho Falls Location

Check if you qualify for this urge urinary incontinence clinical trial in Idaho Falls, ID

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Idaho Falls

    Convenient for ID residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Idaho Falls site if eligible
  4. 4Begin participation

About This Urge Urinary Incontinence Study in Idaho Falls

The purpose of this prospective, multicenter study is to assess the long-term safety and effectiveness of the Altaviva™ system for the treatment of UUI

Sponsor: MedtronicNeuro

Who Can Participate

Inclusion Criteria

Candidate for Altaviva™ therapy per Altaviva™ labeling
Have a diagnosis of UUI as demonstrated on a 3-day voiding diary by having a minimum of 3 episodes of urinary urge incontinence in 72 hours
If taking OAB medications, subjects should be on a stable dose for at least 3 months prior to baseline and willing to remain on stable treatment through completion of the 12-month voiding diary
Patient must be willing and able to accurately complete study questionnaires, attend visits, operate the system, and comply with the study protocol
Willing and able to provide signed and dated informed consent

Exclusion Criteria

Patient who is not a candidate for Altaviva™ therapy per Altaviva™ labeling, including:
Patients who are considered to be poor surgical candidates or who are at risk for poor wound healing per Altaviva™ labeling
Have progressive, systemic neurological disease
Have clinically significant peripheral neuropathy in the lower leg
Severe, uncontrolled diabetes
Have primary stress incontinence or mixed incontinence where the stress component overrides the urge component based on physician judgment
Current symptomatic urinary tract infection
Patients who have been treated with percutaneous tibial nerve stimulation (PTNS)/percutaneous tibial neuromodulation (PTNM) therapy in the past 4 weeks, or longer if the investigator judges that the therapeutic effect is still present
Patients who have had treatment of urinary symptoms with botulinum toxin therapy or sacral neuromodulation in the past 6 months
History of a prior implantable tibial neuromodulation system
Patients who are pregnant or planning to become pregnant during the course of the study
Patient is currently enrolled or plans to enroll in concurrent drug/device study that may confound study results

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Idaho Falls?

Yes, this clinical trial (NCT07456865) has an active research site in Idaho Falls, ID that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Urge Urinary Incontinence Treatment Options in Idaho Falls, ID

If you're searching for urge urinary incontinence treatment options in Idaho Falls, ID, this clinical trial (NCT07456865) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Idaho Falls research site is actively enrolling participants for this clinical trial. You'll receive care from experienced urge urinary incontinence specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all urge urinary incontinence clinical trials near you to find additional studies recruiting in your area.

More Urinary Incontinence Trials in Idaho Falls, ID

See all urinary incontinence clinical trials recruiting in Idaho Falls — not just this study.

Browse Urinary Incontinence Trials in Idaho Falls →

Browse More Trials by Condition

Urinary Incontinence TrialsAll Conditions →

Ready to Join in Idaho Falls?

Take the first step toward participating in this groundbreaking clinical trial

Secure · Expert Care · Idaho Falls, ID