Last updated: August 26, 2025
Sponsor: Centre Hospitalier Intercommunal Creteil
Overall Status: Completed
Phase
N/A
Condition
Lung Injury
Respiratory Failure
Treatment
Survey of sedo-analgesia practices before laryngoscopy
Clinical Study ID
NCT06356909
SUPREMEneo
Ages 20-44 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Every neonate (corrected gestational age < 45 weeks of gestation) that undergoes alaryngoscopy (for intubation or LISA) or a laryngeal mask insertion, that received apremedication or not during the 28 days of the survey.
Exclusion
Exclusion Criteria:
Laryngoscopy or laryngeal mask insertion in the operating room
Opposition to data collection of a parent or holder of parental rights
Study Design
Total Participants: 741
Treatment Group(s): 1
Primary Treatment: Survey of sedo-analgesia practices before laryngoscopy
Phase:
Study Start date:
March 11, 2024
Estimated Completion Date:
April 07, 2024
Study Description
Connect with a study center
Centre Hospitalier Intercommunal de Creteil
Creteil, 94000
FranceSite Not Available
Centre Hospitalier Intercommunal de Creteil
Créteil 3022530, 94000
FranceSite Not Available

Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.