About this trial
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.
Eligibility criteria
Qualifiers
Myelomeningocele (including myeloschisis) at any level from T1 through S1 with hindbrain herniation. Lesion level will be confirmed by ultrasound and hindbrain herniation will be confirmed by MRI at the UC Davis Fetal Center
Maternal age ≥18 years
Gestational age at enrollment between 19 weeks 0 days and 25 weeks 6 days gestation as determined by clinical information and evaluation of first ultrasound
Normal karyotype. Results by fluorescence in situ hybridization (FISH) will be acceptable if the patient is greater than 24 weeks gestation;
Disqualifiers
Multifetal pregnancy
Insulin dependent pregestational diabetes
Fetal anomaly not related to myelomeningocele.
Kyphosis in the fetus of 30 degrees or more
Trial design
Treatments tested in this trial
- Placental Mesenchymal Stem Cells seeded on a commercially available dural graft extracellular matrix
- Untreated contemporaneous cohort
Treatment groups
Sponsors and collaborators
University of California, Davis
Lead sponsor
California Institute for Regenerative Medicine (CIRM)
Collaborator