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NCT03237715

Unbound Bilirubin Levels in Healthy Term and Late Preterm Infants

Status unknown Last updated 2 August 2017
What this trial tests

trial testing Assessment of unbound bilirubin levels in Neonatal Jaundice in 180 participants. Status unknown.

Timeline
1 July 2017
Primary endpoint
30 June 2019
30 June 2019

Quick facts

Lead sponsorRutgers University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment180
Start date1 July 2017
Primary completion30 June 2019
Estimated completion30 June 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Rutgers University

Who can join

Adults 6 Hours to 7 Days, any sex, with Neonatal Jaundice. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Specific Aim 1: To determine total serum bilirubin (TSB) and unbound bilirubin (Bf) levels in term and late preterm infants during the first week of life. Specific Aim 2: Measure Bf levels in breast fed and formula fed infants and examine their relationship to unbound fatty acid (FFAu) levels. Specific Aim 3: To demonstrate that phototherapy results in different changes in TSB and Bf.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Neonatal Jaundice

Currently open trials in the same condition.

Other Rutgers University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03237715.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing