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Clinical Trials/CTRI/2016/12/007536
CTRI/2016/12/007536
Completed
未知

Feasibility and safety of Umbilical cord blood as a potential source for blood transfusion in neonates - Prospective cohort study.

Institute of Child Health and hospital for ChildrenDepartment of Neonatology0 sites200 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- umbilical cord blood collection and storage
Sponsor
Institute of Child Health and hospital for ChildrenDepartment of Neonatology
Enrollment
200
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
Institute of Child Health and hospital for ChildrenDepartment of Neonatology

Eligibility Criteria

Inclusion Criteria

  • Mothers who consent for collection and storage of their Umbilical cord blood at the time of delivery

Exclusion Criteria

  • 1\. Mothers diagnosed with HIV/HBV/HCV/Malaria/Syphilis infection
  • 2\. Mothers who opt for stem cell storage from Umbilical cord blood.

Outcomes

Primary Outcomes

Not specified

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