Dallas, TXNCT06025734Now EnrollingIRB Ready

Spina Bifida Clinical Trial in Dallas, TX

Access cutting-edge spina bifida treatment through this clinical trial at a research site in Dallas. Study-provided care at no cost to qualified participants.

Sponsored by University of Texas Southwestern Medical Center

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Expert Care in Dallas

Access spina bifida specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related spina bifida treatment provided free

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Check if you qualify for this spina bifida clinical trial in Dallas, TX

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

Why Participate?

  • No-Cost Study Care

  • Local to Dallas

    Convenient for TX 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 Dallas site if eligible
  4. 4Begin participation

About This Spina Bifida Study in Dallas

The purpose of this research study is to determine the effectiveness of a treatment called "transcutaneous tibial nerve stimulation" or "TTNS" in the treatment of urinary leakage for patients with spina bifida. This treatment involves electrical stimulation of a nerve by the ankle. Participants will complete urodynamic testing and questionnaires prior to the treatments. Participants will then complete 6 weekly treatments of TTNS. Participants will learn how to do the treatment in the clinic, and then can complete the treatments at home. For patients with a good response, the treatments may be continued for another 6 weeks, for a total of 6 weeks.

Sponsor: University of Texas Southwestern Medical Center

Who Can Participate

Inclusion Criteria

Patient at TSRH
Diagnosis of lumbosacral spina bifida (myelomeningocele, meningocele, lipoma of spinal cord, myelocystocele, diastematomyelia, fatty/thickened filum)
Incontinence refractory to compliant catheterization (compliance with catheterization as assessed by their treating provider)
Patient able and willing to undergo urodynamic testing without sedation
No surgical reconstruction with the exception of a single appendicovesicostomy (APV)
No Botox treatments within 1 year of enrollment
Patient willing and able to stop bladder medications (anticholinergics or beta agonists) 2 weeks prior to pre-intervention bladder diary, questionnaires and UDS
Patient lives close enough to TSRH and CMC to be willing to return for UDS, teaching, and clinic visits as detailed above
Patient/family speak English

Exclusion Criteria

Ages \<8 or \>18
Diagnosis not listed above
Patients that have received reconstructive surgeries (i.e. augmentation or bladder neck sling) with the exception for a single APV
Patient received Botox treatment within 1 year of enrollment
Patient unable or unwilling to stop bladder medications (anticholinergics or beta agonists)
Patients with high-risk bladders, as assessed by their treating provider (i.e. poorly compliant bladders with high end-fill pressures)
Non-English speaking
Patients who are pregnant
Patients who are suspected of being pregnant
Patients who are nursing

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 Dallas?

Yes, this clinical trial (NCT06025734) has an active research site in Dallas, TX 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.

Spina Bifida Treatment Options in Dallas, TX

If you're searching for spina bifida treatment options in Dallas, TX, this clinical trial (NCT06025734) 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 Dallas research site is actively enrolling participants for this clinical trial. You'll receive care from experienced spina bifida 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 spina bifida clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Dallas, TX