NIH-funded research U01 cooperative agreement

Endoscopic versus Shunt Treatment of Hydrocephalus in Infants

Funded at Utah State Higher Education System--University of Utah · NIH-11608585 · Data updated 2026-11-12

A study compares two treatments for hydrocephalus in infants to see which keeps babies cognitively on par with the standard shunt treatment.

More Hydrocephalus research and trials

Quick facts

Grant typeU01 cooperative agreement
Study typeNIH-funded research
Funding institutionUtah State Higher Education System--University of Utah
NIH-funded
Lab location1 site (Salt Lake City, United States)
Project startSeptember 15, 2019
Project endAugust 31, 2027
Funding year2026
Award (this year)$20,739
NIH project number3U01NS107486-07S3
Project IDNIH-11608585 on NIH RePORTER

Who could benefit from this research

Could help

Infants ≤12 months corrected age with hydrocephalus treated at participating tertiary pediatric neurosurgery centers in North America.

Less likely to help

Infants for whom ETV+CPC is not feasible or fails to meet cognitive non-inferiority criteria may not experience a benefit.

What this research studies

This project looks at infants under one year with hydrocephalus and compares endoscopic third ventriculostomy with choroid plexus cauterization (ETV+CPC) against the traditional CSF shunt. It is designed as a multicenter effort across North American pediatric neurosurgery centers to measure cognitive outcomes 12 months after treatment using the Bayley Scales of Infant and Toddler Development. The goal is to determine if ETV+CPC is not worse than shunt by a small margin, potentially offering a shunt-free option for families. The study will inform clinicians and families about risks, benefits, and long-term cognitive expectations of each approach.

Why it matters

Potential benefit: If successful, the research could support safer, shunt-free options for infants with hydrocephalus and improve long-term cognitive outcomes.

How similar studies have gone: Previous studies suggest ETV+CPC is safe and viable, but cognitive outcomes relative to shunt require clarification in a larger, non-inferiority trial.

Where this research is happening

  • Utah State Higher Education System--University of Utah
    Salt Lake City, United States
    Active

Researchers

  • Principal investigator: Kestle, John — Utah State Higher Education System--University of Utah
  • Study coordinator: Kestle, John

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.