CompletedNot Applicable

Study of PREMEdication Before Laryngoscopy in Neonates in France

France741 participantsStarted 2024-03-11

Plain-language summary

This study is a national prospective survey on practices of premedication before laryngoscopy in neonates. The survey will evaluate adequation to the French best practice guidelines to improve their dissemination and to identify current practices of premedication before laryngoscopy in neonates in French units (agents, dosing, efficacy, safety)

Who can participate

Age range20 Weeks – 44 Weeks

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Every neonate (corrected gestational age \< 45 weeks of gestation) that undergoes a laryngoscopy (for intubation or LISA) or a laryngeal mask insertion, that received a premedication or not during the 28 days of the survey. Exclusion Criteria: * Laryngoscopy or laryngeal mask insertion in the operating room * Opposition to data collection of a parent or holder of parental rights

What they're measuring

Proportion of patients who received a 1st sequence of sedo-analgesia consistent with best practice guidelines during laryngoscopy or laryngeal mask placement

Timeframe: Immediately after the laryngoscopy

Trial details

NCT IDNCT06356909

SponsorCentre Hospitalier Intercommunal Creteil

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-04-07

View on ClinicalTrials.gov More Neonatal Respiratory Distress trials