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UnknownNCT05138276

Effect of Autologous Cord Blood Mononuclear Cells for Digestive System in Preterm Neonates

Status
Unknown
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Guangdong Women and Children Hospital · Academic / Other
Sex
All
Age
26 Weeks – 32 Weeks
Healthy volunteers
Not accepted

Summary

Pre-clinical animal studies provide robust evidence regarding the beneficial effect of stem cells for intestinal disease. This single-center, randomized, controlled, blinded trial assessed the effect of a single intravenous infusion of autologous cord blood MNCs (ACBMNCs) in preventing NEC in preterm neonates,and influence on growth and development.

Detailed description

Study design and settings: This study will be a randomized, placebo-controlled, double-blinded, single-center trial. A total of 45 singleton preterm infants (GS\<33 weeks) of fulfilling the eligibility criteria will be enrolled. According to the infusion of umbilical cord blood mononuclear cells and equal dose placebo, the premature infants were divided into infusion group and control group. The two groups were matched with gender, gestational age and birth weight as stratified variables and 1:2 (the gender was the same, and the difference between gestational age and birth weight was the smallest). Trial treatment methods: Study design and settings: This study will be a randomized, placebo-controlled, double-blinded, single-center trial. A total of 30 pairs of monozygotic twins fulfilling the eligibility criteria will be enrolled. Subsequently, one baby of each twin will be randomly divided into the ACBMNC infusion group or control (placebo) group. Trial treatment methods: Soon after the preterm infant was deliveried, written consent was signed by the parents, and autologous cord blood infusion was applied to the baby in addition to routine treatment. Those assigned to the ACBMNC group received an infusion of ACBMNC . Those in control group received an infusion of a placebo solution. Informed consent before birth is signed. Preterm infants in the ACBMNC infusion group will have their umbilical cord blood collected after birth, and then their umbilical cord blood will be separated through Guangdong Province umbilical cord blood Bank to obtain mesenchymal stem cells. Within 24h after birth, ACBMNC group received an infusion of mesenchymal stem cells timely, while control (placebo) group received an infusion of a placebo solution which is normal saline with the same volume. Cell dose for all patients was targeted at 5×107 cells per kilogram.

Conditions

Interventions

TypeNameDescription
OTHERAutologous Umbilical Cord Blood Mononuclear Cells TherapyAutologous Umbilical Cord Blood Mononuclear Cells Therapy in preterm for prevention of NEC
DRUG0.9% Sodium Chloride0.9% Sodium Chloride in control group

Timeline

Start date
2021-09-01
Primary completion
2022-12-31
Completion
2022-12-31
First posted
2021-11-30
Last updated
2022-04-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05138276. Inclusion in this directory is not an endorsement.