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BUBOLight®, a New Phototherapy Device for the Treatment of the Newborn's Jaundice
Sponsor: University Hospital, Lille
Summary
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.
Official title: Use of "BUBOLight®" Device as an Innovative Phototherapy Device for the Treatment of Newborn's Jaundice. A Monocentric, Descriptive Pilot Study, for the Feasibility, Safety and Tolerance of the BUBOLight® Device
Key Details
Gender
All
Age Range
Any - 30 Days
Study Type
INTERVENTIONAL
Enrollment
15
Start Date
2020-10-08
Completion Date
2026-12
Last Updated
2025-12-23
Healthy Volunteers
No
Conditions
Interventions
BUBOLight® Device
1 session of phototherapy with BUBOLight® device during 4 hours.
Locations (1)
Hop Jeanne de Flandre Chu Lille
Lille, France