Vinmec International Hospital
Hanoi, Vietnam
NCT Number: NCT02569775
The aim of this study is to assess the safety and effectiveness of autologous bone marrow mononuclear stem cells in patients with cerebral palsy.
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Notify Me1 year–15 year
All sexes
Interventional
Phase 2
Hanoi, Vietnam
The aim of this study is to assess the safety and effectiveness of autologous bone marrow mononuclear stem cells in 40 patients with cerebral palsy at Vinmec International Hospital, Hanoi, Vietnam.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Transplantation of Autologous Bone Marrow Mononuclear Cells
Time frame: 3 months and 6 months after transplantation
GMFM-88
Time frame: 3 months and 6 months after transplantation
GMFM-66 percentile
Time frame: 3 months and 6 months after transplantation
Muscle tone are assessed by Modified Ashworth Scale
Time frame: Through study completion, an average of 6 months
Examples of adverse events to look for: anaphylaxis, allergy, respiratory distress, fever, infections, vomit, epilepsy
Vinmec Healthcare System
Other
Outcomes of Autologous Bone Marrow Mononuclear Cells for Cerebral Palsy: A Self-Controlled Clinical Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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