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Optimization of Ventilation Strategies in Preterm and Term Infants in a Single-center Intervention Study

NCT05512689 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2023-11-22

No results posted yet for this study

Summary

This study was a non-blinded, non-randomized intervention study in a single-center clinical setting, analyzing ventilation quality with and without RFM visibility.

Conditions

  • Lung-protective Ventilation
  • Respiratory Function Monitor

Interventions

DEVICE

Ventilations while using a respiratory function monitor

Healthcare professionals are able to use a feedback device to guide their ventilations.

Sponsors & Collaborators

  • Medical University of Vienna

    lead OTHER

Principal Investigators

  • Michael Wagner, MD PhD · Medical University of Vienna

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SEQUENTIAL

Eligibility

Max Age
12 Months
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-01
Primary Completion
2023-03-01
Completion
2023-03-01

Countries

  • Austria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05512689 on ClinicalTrials.gov