Feasibility and safety of Umbilical cord blood as a potential source for blood transfusion in neonates.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- umbilical cord blood collection and storage
- Registration Number
- CTRI/2016/12/007536
- Lead Sponsor
- Institute of Child Health and hospital for ChildrenDepartment of Neonatology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 200
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.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Quantity of umbilical cord blood (ml) that can be collected per neonate across different gestational age, birth weight, mode of delivery and collection method 2. Change in Parameters of collected and stored <br/ ><br>umbilical cord blood <br/ ><br>â?¢ pH (0, 7, 14, 21, 30 days) <br/ ><br>â?¢ Potassium (0, 7,14,21,30 days) <br/ ><br>â?¢ Haematocrit (0, 7,14,21,30 days) <br/ ><br>â?¢ Free Haemoglobin (0, 14, 28days) <br/ ><br>â?¢ Cord blood culture (0,14 days) <br/ ><br> <br/ ><br>Timepoint: 0, 7, 14, 21, 30 days
- Secondary Outcome Measures
Name Time Method Quantity of packed RBC(ml) that can be <br/ ><br>separated from the umbilical cord blood after <br/ ><br>collection.Timepoint: day 1