NIH-funded research U01 cooperative agreement

Urology care plan for children born with spina bifida

Official title: Comp C Spina Bifida Urologic Protocol at Vanderbilt Children's Hospital

Funded at Vanderbilt University Medical Center · NIH-11400829 · Data updated 2026-11-12

Using a standardized urology care plan for newborns and children with spina bifida to help protect kidneys and improve bladder control.

More Spina Bifida research and trials

Quick facts

Grant typeU01 cooperative agreement
Study typeNIH-funded research
Funding institutionVanderbilt University Medical Center
NIH-funded
Lab location1 site (Nashville, United States)
Project startSeptember 1, 2019
Project endAugust 31, 2026
Funding year2023
Award (this year)$25,000
NIH project number6U01DD001234-05M002
Project IDNIH-11400829 on NIH RePORTER

Who could benefit from this research

Could help

Newborns and young children (up to about 10 years of age) with spina bifida who are followed through Vanderbilt's Spina Bifida Program are the ideal candidates.

Less likely to help

Adults, people without spina bifida, or children who already have severe, irreversible kidney damage are unlikely to benefit from this protocol.

What this research studies

If your child was born with spina bifida, this protocol follows them from the newborn period up to age 10 with regular urology checks and tests. Vanderbilt clinicians collect detailed, long-term information on imaging, bladder studies (including videourodynamics), treatments, and outcomes. The team aims to use the same care steps across patients so they can spot clinical signs that predict kidney problems or difficult bladder function. Data are entered and quality-controlled for contribution to the UMPIRE effort and shared with the broader UMPIRE network to guide better care.

Why it matters

Potential benefit: If successful, the protocol could help doctors choose care that better preserves kidney function and improves bladder continence for children with spina bifida.

How similar studies have gone: Related UMPIRE work from participating centers has produced published data and helped inform care, although longer-term outcomes are still being clarified.

Where this research is happening

  • Vanderbilt University Medical Center
    Nashville, United States
    Active

Researchers

  • Principal investigator: Clayton, Douglass Brooks — Vanderbilt University Medical Center
  • Study coordinator: Clayton, Douglass Brooks

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.