Necrotizing Enterocolities

ConditionNecrotizing Enterocolitis of Newborn

Trial statusNot yet recruiting

Trial phaseNot listed

Trial typeObservational

Biological sexAll

Age1-30

SponsorAssiut University

About this trial

Haematological disturbances in neonates with necrotizing enterocolities

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

preterm less than 36 weeks

Or very low birth weight less than 1500 gram

Disqualifiers

full term

Normal birth weight ,Preterm with early breast feeding or more than 1500 gm

Trial population

Neonates with necrotizing enterocolities

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Complete blood count
Diagnostic test
Study haemtological disturbances in neonates with necrotizing enterocolities
Complete blood count
Other intervention
Haemtological disturbances in neonates with necrotizing enterocolities

Treatment groups

70 Participants

are divided into 1 treatment group

Group A: Neonates with necrotizing enterocolities2 interventions

Trial outcomes

Primary outcomes

Aim

:to delineate haemtological abnormalities in neonatal necrotizing enterocolities as predictors of morbidity and mortality

Time frame

Baseline

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Assiut University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: