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Clinical Trials/NCT04723966
NCT04723966UnknownNot Applicable

Safety and Efficacy Evaluation of TPN in Preterm Neonates in NICU of Cairo University Children Hospital

Cairo University1 site in 1 country200 target enrollmentStarted: April 7, 2019Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
200
Locations
1
Primary Endpoint
electrolyte and mineral disturbance associated with TPN in preterm receiving it
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The aim of this work is evaluation of electrolytes and minerals homeostasis and occurrence of complications among preterm babies receiving total parenteral nutrition, and admitted to the neonatal intensive care units of Cairo University Children hospitals.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
1 Day to 1 Month (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •All preterm infants with gestational age < 34 weeks, Receiving total parenteral nutrition. Normal serum magnesium.

Exclusion Criteria

  • •Any full-term neonates Any patient with TORCH infection, chromosomal, metabolic disorders or surgical abnormality of the hepatobiliary system

Outcomes

Primary Outcomes

electrolyte and mineral disturbance associated with TPN in preterm receiving it

Time Frame: 14 days

NA, K, MG, P, CA.

Secondary Outcomes

  • prevalence of cholestasis and sepsis in preterm receiving TPN(14 days)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Khalid Mohammed Shehata

doctor

Cairo University

Study Sites (1)

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