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Study identifier: NCT02881970 Synced from ClinicalTrials.gov · July 29, 2026
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Neonatal Hypoxic Ischemic Encephalopathy : Safety and Feasibility Study of a Curative Treatment With Autologous Cord Blood Stem Cells

Condition: Neonatal Hypoxic-ischaemic Encephalopathy  ·  Sponsor: Assistance Publique Hopitaux De Marseille

PhasePhase 1/Phase 2
Planned participants20
Who can joinAll sexes, 1 Day to 3 Days
Healthy volunteersNo

About this study

Neonatal hypoxic-ischaemic encephalopathy is a dramatic perinatal complication due to brain asphyxia. Neurological and neurosensory sequelae are frequent in survivors, due to neuronal damage and loss. Currently, only total or partial body hypothermia can partially prevent cell loss. However, no treatment exists to restore neuronal functions. Cord blood stem cells are a promising treatment for the near future. The primary objective of this study is to test the safety and feasibility of a curative treatment with autologous cord blood stem cell in neonatal hypoxic-ischaemic encephalopathy. The secondary objectives are to test the efficacy of this curative treatment with cell with neurogenic potential on the prevention of neurologic sequelae, as well as to test the optimum timing of cell preparation administration

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

Talk to the study team

Farid BOUBRED  ·  farid.boubrd@ap-hm.fr

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Locations (1)

Assistance Publique Hopitaux de MarseilleMarseille, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT02881970