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Role of Interleukin-1β and Prostaglandin E2 in Prediction and Outcome of Apnea in Neonates

Role of Interleukin-1β and Prostaglandin E2 in Prediction and Outcome of Apnea in Neonates

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06827197
Enrollment
100
Registered
2025-02-14
Start date
2023-05-01
Completion date
2023-10-30
Last updated
2025-02-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature Newborns, Premature Newborns With Gestational Age 28 to 33 Weeks

Keywords

Apnea of prematurity, Interleukin-1β, Prostaglandin E2, Outcome

Brief summary

Our thesis proposed that IL-1β may affect brainstem respiratory control via prostaglandin-dependant mechanism so we investigated the mediator roles of IL-1β and PGE2 levels in predicting apnea in pretertm newborn and their relation to clinical outcomes.

Interventions

DIAGNOSTIC_TESTBlood test

Blood samples were withdrawn from all the neonates under strict aseptic conditions and stored at -80°C for detecting PGE2 and IL-1β levels. PGE2 and IL-1β concentrations were measured using ELISA.

Sponsors

Benha University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to 2 Months
Healthy volunteers
No

Inclusion criteria

* Preterm infants born at less than 37 weeks of gestation. * Neonates aged from birth up to 28 days. * Neonates diagnosed with apnea of prematurity or exhibiting apneic episodes

Exclusion criteria

* Full-term neonates. * Neonates with major congenital malformations or genetic syndromes. * Neonates with severe neurological impairments (e.g., intraventricular hemorrhage grade III or IV). * Neonates with confirmed or suspected sepsis or active infections. * Neonates receiving steroids, nonsteroidal anti-inflammatory drugs (NSAIDs), or other medications known to alter interleukin-1β or prostaglandin E2 levels. * Neonates with congenital heart diseases. * Neonates with a history of significant birth asphyxia requiring extensive resuscitation. * Neonates whose parents or guardians refuse to provide informed consent.

Design outcomes

Primary

MeasureTime frame
Duration of NICU stay1 month
Mortality rate1 month

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026