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mbilical cord blood collected from term babies for transfusion in premature babies

Phase 3
Conditions
Health Condition 1: D648- Other specified anemias
Registration Number
CTRI/2019/11/021886
Lead Sponsor
Intramural GATE Research fund from SRIHER
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. For collection of UCB - Term (>=37 weeks gestation) infants delivered by elective caesarean section

2. For transfusion of UCB - Premature infants <1500 g birth weight requiring transfusion during the NICU stay

Exclusion Criteria

For collection of UCB

1. Mothers positive for HIV, HBsAg, HCV or VDRL

2. Mothers positive for unusual RBC antibodies screen

3. Mother who opt for cord blood banking

4. Maternal-fetal iso-immunization

5. Lack of consent

For transfusion of UCB

1. UCB compatible with babyâ??s blood not available

2. Lack of consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion of red cell concentrates (RCC) transfusions in preterm infants that are covered by UCBTimepoint: Until discharge from the NIC
Secondary Outcome Measures
NameTimeMethod
1. Success rate of UCB collection after DCC (defined as absolute UCB volume â?¥ 25 mL) <br/ ><br>2. Volume of UCB collected/volume of RCC obtained <br/ ><br>3. Proportion of UCB units with satisfactory quality based on microbiological, hematological <br/ ><br>and biochemical parameters available until 21 days of storage.Timepoint: 21 days of storage (maximum)
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