ASSESSMENT OF PAIN AND DISCOMFORT DURING LESS INVASIVE SURFACTANT ADMINISTRATIO

• Conditions: P07.1; P22.0; P07.0; Respiratory distress syndrome of newborn; Extremely low birth weight; Other low birth weight

• Registration Number: DRKS00022317
• Lead Sponsor: eonatologie der Medizinischen Universität Wien

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-09-07
• Study Completion: 2021-09-03
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 115

Inclusion Criteria

Preterm infants =32+0 weeks of gestation born at the Department of Neonatology of the Medical University Vienna, Austria or Cologne University hospital, Germany with RDS and the need for surfactant replacement will be included in the study.

Exclusion Criteria

Exclusion criteria will be infants with major congenital malformations/syndromes as well as conditions that do not allow LISA but require emergency intubation such as severe haemodynamic compromise, pneumothorax or prolonged apnea >2 min.

Study & Design

• Study Type: observational
• Study Design: Not specified