Outcome of Intraventricular Hemorrhage in Preterm Infants
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 28
SponsorAssiut University
About this trial
To determine the incidence and grading of IVH among preterm neonates in the NICU.
* To identify maternal and neonatal risk factors associated with IVH. * To assess short-term outcomes (mortality, Hydrocephalus, need for neurosurgical intervention, seizures, length of Hospital stay).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Preterm neonates < 34 weeks of gestation
Birth weight < 1500g
Admitted to NICU within 24 hours of birth
Disqualifiers
Major congenital malformations (especially CNS anomalies)
Severe perinatal asphyxia
Neonates with congenital infections (TORCH)
Trial population
All with the required Criteria
Trial design
Design model
Other
Time perspective
Prospective
Treatments tested in this trial
No intervention
Other interventionNot found
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
. To determine the incidence of IVH in preterm infants within the first 7 days of life using cranial ultrasound. . To assess the grade of IVH (Papile classification I-IV) in preterm infants based on cranial US findings.
Outcome of intraventricular haemorrhage in preterm infants
Time frame
BaselineLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: