Serum Erythropoietin Level in Perinatal Asphyxia

NCT05018364 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2021-08-30

No results posted yet for this study

Summary

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

Conditions

  • Perinatal Hypoxia

Interventions

DIAGNOSTIC_TEST

Serum erythropoietin level

Evaluate serum erythropoietin level in neonates exposed to hypoxia compared to control group

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

Eligibility

Min Age
1 Day
Max Age
4 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-08-01
Primary Completion
2021-06-01
Completion
2021-06-15

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05018364 on ClinicalTrials.gov