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Ceftriaxone and Jaundice in Neonates

Effect of Ceftriaxone on Neonatal Jaundice

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03133637
Acronym
CEFT
Enrollment
27
Registered
2017-04-28
Start date
2016-03-31
Completion date
2019-08-31
Last updated
2021-04-06

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

Conditions

Jaundice and Sepsis in Neonates

Brief summary

Ceftriaxone is an antibiotic often used for the management of sepsis. Neonates commonly have jaundice during the first postnatal week. Ceftriaxone will be given as standard of care for sepsis and investigators will observe the effect on jaundice.

Interventions

DRUGceftriaxone

Eligible infants will receive ceftriaxone as standard of care for sepsis

Sponsors

University of Rochester
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Days to 7 Days
Healthy volunteers
No

Inclusion criteria

* Term infants with sepsis requiring IV antibiotics for more than 3 days and who has total serum bilirubin 6-12 mg/dL and resolving by day 4 of life.

Exclusion criteria

* Infants with asphyxia (Apgar score \<3 at 5 minutes), chromosomal disorder, failed hearing test at baseline, family history of hearing loss, unconjugated hyperbilirubinemia requiring phototherapy, TORCH infection, craniofacial malformations, listeria monocytogenes infection, and any clinical conditions which will preclude discharge to home.

Design outcomes

Primary

MeasureTime frame
change in bilirubin binding assaysbaseline and through study completion, an average of 1 hour

Secondary

MeasureTime frame
Automated brain stem evoke response testthrough study completion, an average of 1 hour

Countries

United States

Outcome results

None listed

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