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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05163145
Other study ID # neonates receiveTPN
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 1, 2022
Est. completion date March 2, 2023

Study information

Verified date May 2022
Source Assiut University
Contact Mayyada ElsayedMohamed, resident
Phone 01002686656
Email soadalsayed2@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate the risk factors of PNAC in neonates


Description:

Neonates with prematurity,gastrointestinal dysfunction and very low birth weights are often intolerant to oral feeding.In such infants,the provision of nutrients via parenteral nutrition (PN)becomes necessary for short term survival,as well as long-term health. Wilmore and Dudrick first reported use of parenteral nutrition(PN) for an infant more than 40years ago Soon there after physicians recognized that PN was associated with significant liver changes.In the first reported case of parenteral nutrition-associated conjugated hyperbilirubinemia (PNAC) in a premature infant hepatomegaly was noted on the18thday of fat-free PN and worsened until death on the71st day of life The hyperbilirubinemia manifest in PNAC is thought to occur from impaired hepatic bileflow, an adynamic gallbladder,and an upsurge in release of conjugated bilirubin as an infant matures.Atbirth,preterm neonates havereduced activity of the uridine diphosphate glucuronosyl transferase1A1 liver enzyme(UDPGT)that catalyzes conjugation of bilirubin As the infant develops,UDPGT becomes more functional, increasing hepatocyte efficiency for conjugation.Thus,in combination with cholestasis,and neonatal intestinal absorption of unconjugated bilirubin,more conjugated bilirubin is made available to pass from the liver into circulation. Parenteral nutrition associated cholestasis (PNAC) is the most common form of liver damage in neonates while receiving parenteral nutrition(PN).Its prevalence was reported between10%and 60%in NICU Cholestasisis acommonly described complication of PN. Its etiology is not fully understood and is thought to be multifactorial Proposed mechanisms included altered bile salt metabolisms secondary to prematurity and toxic effect of PN components on the liver the presence or absence of specific components in parenteral nutrition solutions most certainly contributing to the disease mechanism,and gastrointestinal systems .Aggravating factors such as sepsis and duration of bowel rest have also been described


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date March 2, 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A to 28 Days
Eligibility Inclusion Criteria: - Neonates who received PN for =14 days Exclusion Criteria::Neonates with major congenital anomaly, cholestasis at birth,diseases associated with cholestasis (i.e.,inborn errors of metabolism,viral hepatitis,cystic fibrosis and any primary cholestatic liver diseases)that were diagnosed while hospitalized.the possibility of surgical causes of conjugated hyperbilirubinemia(such as biliary atresia,choledochalcyst on abdominal ultrasonography,and hepatobiliary scintigraphy -

Study Design


Related Conditions & MeSH terms


Intervention

Other:
TPN
early detection of comlications of prolonged TPN on neonatal liver

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Mayyada Elsayed Mohamed Hussien

Outcome

Type Measure Description Time frame Safety issue
Primary effect of TPN on neonatal liver TPN associated cholestasis in neonates baseline
See also
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Recruiting NCT03842150 - Development and Validation of a Screening Score for the Biliary Atresia in Infantile Cholestasis: A Prospective Study
Completed NCT01875510 - The Influence of Fish-oil Lipid Emulsions on Neonatal Morbidities N/A
Recruiting NCT00061828 - A Prospective Database of Infants With Cholestasis
Not yet recruiting NCT03898765 - Dry Blood Spot Screening Test for Biliary Atresia(DBS-SCReBA) N/A