Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT04365998
NA

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

Sponsor: University Hospital, Lille

View on ClinicalTrials.gov

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

Interventions

DEVICE

BUBOLight® Device

1 session of phototherapy with BUBOLight® device during 4 hours.

Locations (1)

Hop Jeanne de Flandre Chu Lille

Lille, France