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Study identifier: NCT04652908 Synced from ClinicalTrials.gov · July 29, 2026
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Cellular Therapy for In Utero Repair of Myelomeningocele - The CuRe Trial

Condition: Myelomeningocele  ·  Sponsor: University of California, Davis

PhasePhase 1/Phase 2
Planned participants55
Who can joinAll sexes, 19 Weeks to 25 Weeks
Healthy volunteersNo

About this study

Spina bifida, or myelomeningocele (MMC), is a birth defect that results in paralysis, excess fluid on the brain (hydrocephalus), and impaired ability to urinate and have bowel movements normally. In a previous study (the MOMS trial), surgery before birth (in-utero/fetal surgery) was shown to reduce the need for shunting for hydrocephalus. There was also some improvement in ambulation, but 58 % of the children still could not walk unassisted. This study is testing living stem cells from placenta added to the fetal repair in an effort to improve the ability to walk. Previous animal studies have shown dramatic improvement in walking and bowel and bladder function when placental stem cells are added to MMC repair. Use of these "living" cells may protect the developing spinal cord, prevent further injury, and may even reverse existing damage to the nerves that control movement. This study is assessing the safety and efficacy of adding stem cells to open fetal surgery for MMC in humans.

This description comes directly from the study's public registry record.

Talk to the study team

Amy B Powne, MSN, RN  ·  916-794-2229  ·  fctc@health.ucdavis.edu

Maria G Hernandez  ·  916-734-4156  ·  mghernandez@health.ucdavis.edu

Always discuss trial participation with your own doctor first.

Locations (1)

UC Davis HealthSacramento, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04652908