Clinical Trials Directory

Trials / Completed

CompletedNCT05018364

Serum Erythropoietin Level in Perinatal Asphyxia

Serum Erythropoietin Level for Detection of Kidney and Brain Injuries in Asphyxiated Neonates in Neonatal Intensive Care Unit.

Status
Completed
Phase
Study type
Observational
Enrollment
80 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
1 Day – 4 Days
Healthy volunteers
Accepted

Summary

This study is to evaluate brain and kidney injuries in full-term neonates with perinatal asphyxia by detecting specific biomarker in blood (Erythropoietin).

Detailed description

Perinatal hypoxic-ischemic encephalopathy (HIE) is an important cause of brain injury in the newborn and can result in long-term devastating consequences. Acute kidney injury (AKI) occurs in (50 - 72%) among asphyxiated term infants. The kidney cells that make erythropoietin are sensitive to low oxygen levels in the blood that travels through the kidney. These cells make and release erythropoietin when the oxygen level is too low.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTSerum erythropoietin levelEvaluate serum erythropoietin level in neonates exposed to hypoxia compared to control group

Timeline

Start date
2020-08-01
Primary completion
2021-06-01
Completion
2021-06-15
First posted
2021-08-24
Last updated
2021-08-30

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05018364. Inclusion in this directory is not an endorsement.