Home › Cerebral Palsy › NCT05018871
Safety of Cultured Umbilical or Placental Derived Mesenchymal Stem Cell Intravenous Infusion for CP
RecruitingPhase 1
Safety of Cultured Umbilical or Placental Derived Mesenchymal Stem Cell Intravenous Infusion for the Treatment of Cerebral Palsy
Who can join
All ages · All sexes
Full eligibility criteria
Inclusion Criteria: * Diagnosis of Cerebral Palsy Exclusion Criteria: * Active infection * Active cancer * Chronic multisystem organ failure * Pregnancy * Clinically significant Abnormalities on pre-treatment laboratory evaluation * Medical condition that would (based on the opinion of the investigator) compromise patient's safety * Previous organ transplant * Seizure disorder * Hypersensitivity to sulfur
About the study
This trial will study the safety and efficacy of intravenous infusion of cultured umbilical or placental derived mesenchymal stem cells for the treatment of Cerebral Palsy
What is being tested
- Umbilical or placental derived mesenchymal stem cells (biological)
Sponsor: The Foundation for Orthopaedics and Regenerative Medicine · Participants: 15 · Started: 2026-12
Contact the study team
- Chadwick Prodromos, MD · Phone: 847-699-6810
Official record on ClinicalTrials.gov — NCT05018871
Locations in the U.S.
| Florida | Prodromos Stem Cell Institute, Naples |
Conditions
From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.