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Clinical Trials in Denmark / NCT06702241
Recruiting Phase 2/3

Newborn Jaundice - An Investigation of Different Approaches to Light Therapy

NCT06702241 · tracked via the Priya Life Science Denmark tracker
Phase
Phase 2/3
Started
2025-01-14
Last updated
2025-11-20

Condition(s) studied

Neonatal Hyperbilirubinemia

Investigational drug(s) / intervention(s)

Continuous Phototherapy with a irradiance of 40 µW/cm2/nm from the overhead lightContinuos Phototherapy with a irradiance of 55 µW/cm2/nm from the overhead lightContinuous Phototherapy with a irradiance of 70 µW/cm2/nm from the overhead lightCycled phototherapy with a irradiance of 70 µW/cm2/nm from the overhead light

Continuous Phototherapy with a irradiance of 40 µW/cm2/nm from the overhead light: The difference in irradiance between the groups will be measured with a radiometer specific to the device's wavelength.

Continuos Phototherapy with a irradiance of 55 µW/cm2/nm from the overhead light: The difference in irradiance between the groups will be measured with a radiometer specific for the device's wavelenght

Continuous Phototherapy with a irradiance of 70 µW/cm2/nm from the overhead light: The difference in irradiance between the groups will be measured with a radiometer specific for the device's wavelenght

Cycled phototherapy with a irradiance of 70 µW/cm2/nm from the overhead light: The difference in irradiance between the groups will be measured with a radiometer specific for the device's wavelenght

Study summary

Background Neonatal jaundice affects about 60% of full-term newborns in their first week. If untreated, it can lead to permanent brain damage. In Denmark, 2-5% of newborns require phototherapy, the standard treatment. The maximum beneficial irradiance limit for phototherapy remains unclear. Furthermore, studies suggest that cycled phototherapy is as effective as continuous treatment.

This study aims to investigate the efficacy of elevating the irradiance of intensive phototherapy treatment regimens. This is to evaluate the dose-response relationship. Furthermore, the study aims to compare intermittent phototherapy to continuous phototherapy.

Methods:

In a clinical randomized multicenter trial 116 newborns with non-hemolytic hyperbilirubinemia, gestational age \>33+0, weight \>1800g and no other significant neonatal diagnose will be randomized. All infants will receive 12 hours double therapy with a biliblanket and overhead light providing an intensity of either 40-, 55- or 70 µW/cm2/nm. Three groups will be treated with continuous phototherapy while a fourth group will receive intermittent phototherapy of 1,5 hours cycled intervals with an intensity of 70 µW/cm2/nm.

Parental experiences during treatment will be examined through a survey post treatment.

The study has been approved by the Regional Research Ethics Committee.

Perspectives:

Understanding the dose-response relationship of phototherapy will give an insight in the most effective way of treating neonatal jaundice. Intermittent therapy, if proven non-inferior, could facilitate more intimacy in the parent-infant relationship as well as benefits in initiating breastfeeding

Eligibility

Sex
ALL
Min age
1 Day
Max age
14 Days
Healthy volunteers
No
Inclusion Criteria: * Hyperbilirubinemia with a total serum bilirubin level above the limit of necessary treatment according to the Danish Pediatric Society's guidelines * Birth weight \>1800g * Gestational age \>33+0 Exclusion Criteria: * Hyperbilirubinemia within the first 24 hours of life * Rapidly increasing serum levels of bilirubnemia indicating pathology or hemolysis

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Aalborg University Hospital, The Neonatal Department Aalborg Denmark Recruiting
The North Denmark Regional Hospital, The Pediatric Department Hjørring Denmark Recruiting

More Regionshospital Nordjylland trials in Denmark

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06702241 on ClinicalTrials.gov ↗ ← All trials in Denmark