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Study identifier: NCT04365998 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

BUBOLight®, a New Phototherapy Device for the Treatment of the Newborn's Jaundice

Condition: Neonatal Jaundice  ·  Sponsor: University Hospital, Lille

PhaseNA
Planned participants15
Who can joinAll sexes, N/A to 30 Days
Healthy volunteersNo

About this study

About 50% of full-term newborns and 80% of premature infants develop jaundice which is due to hyperbilirubinemia. In the majority of cases, jaundice disappears naturally without treatment within three weeks of birth, but the bilirubin level may remain too high, which can lead to a serious neurological disease: kernicterus. To avoid this, a therapeutic management must be instituted, and in some cases, one or more phototherapy sessions (PT) may be prescribed. The aim of this trial is to evaluate the safety and level of satisfaction of parents and healthcare team with one innovative device for phototherapy BUBOLight® included two removable strips of luminous textile incorporating optical fibers. 10 newborns requiring phototherapy, will be illuminated during four hours in one session of PT Bilirubin levels is taken at the start of phototherapy H0 and Controls are made at H+6 hours.

This description comes directly from the study's public registry record.

Talk to the study team

Thameur Rakza, MD  ·  03 20 44 63 87  ·  thameur.rakza@chru-lille.fr

Serge Mordon, PhD  ·  serge.mordon@inserm.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Hop Jeanne de Flandre Chu LilleLille, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT04365998