Evaluation of Placental Transfusion Techniques in Prevention of Prematurity Related Complications and Effect on Their Hematological Profile
Recruiting
N/AInterventional Study
PrematurePlacental Transfusion
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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At a Glance
Age
1 Minute – 2 Minutes
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
160 (estimated)
Sponsor
Alexandria University · Other
Who this trial is looking for
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The objective of this study is to evaluate the general course and prognosis associated with different methods of placental transfusion (Intact umbilical cord milking, cut- umbilical cord milking and delayed cord clamping) in premature neonates over the first days of life
Trial Locations
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Eligibility Criteria
* Inclusion Criteria:
1. Premature neonates ≤ 32 weeks gestational age regardless birth weight
2. patients should be admitted to neonatal intensive care unit in the first day of life of life
Exclusion criteria:
* Exclusion Criteria:
Patient with any of the following will be excluded:
1. Maj…
* Inclusion Criteria:
1. Premature neonates ≤ 32 weeks gestational age regardless birth weight
2. patients should be admitted to neonatal intensive care unit in the first day of life of life
Exclusion criteria:
* Exclusion Criteria:
Patient with any of the following will be excluded:
1. Major congenital anomalies (complex cyanotic heart disease, major central nervous system anomalies).
2. Evidence of head trauma causing major intracranial hemorrhage.
3. placental abnormalities like : abruptions, placenta previa or retroplacental hematoma.
4. Cord accident, or avulsion at the time of delivery.
5. Refusal to perform the intervention by the obstetrician
Contacts
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