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Neonatal Respiratory Distress clinical trials

View clinical trials related to Neonatal Respiratory Distress.

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NCT ID: NCT06372951 Not yet recruiting - Clinical trials for Neonatal Respiratory Distress

Lung Ultrasound in Neonatal Intensive Care Units

Start date: May 1, 2024
Phase:
Study type: Observational

Identification of lung diseases causing neonatal respiratory distress by lung ultrasound as a tool that can replace x-ray .

NCT ID: NCT06356909 Recruiting - Clinical trials for Neonatal Respiratory Distress

Study of PREMEdication Before Laryngoscopy in Neonates in France

SUPREMEneo
Start date: March 11, 2024
Phase:
Study type: Observational

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)

NCT ID: NCT06292338 Not yet recruiting - Clinical trials for Neonatal Respiratory Distress

Lung Sonar in Neonatal Respiratory Disorders

Start date: May 1, 2024
Phase:
Study type: Observational

This study aimed to determine the value of chest ultrasonography in comparison to other tools as chest x-ray and ABG in diagnosis and follow up of neonates with respiratory disorders.

NCT ID: NCT06285669 Completed - Clinical trials for Respiratory Distress Syndrome

Effects of Kinesiotaping on Respiratory Muscles in Very Preterm Infants

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

This study aimed to evaluate the effects of kinesio taping on blood gas parameters, respiratory rate, heart rate, oxygen saturation, and pressure limits in preterm infants with RDS who are on NIV. It is hypothesized that the application of kinesio taping to the chest area of preterm infants may improve respiratory functions and oxygenation at the alveolar level, leading to decreased work of breathing, reduced respiratory rate, and improved neonatal stability by promoting respiratory mechanics and enhancing chest expansion.

NCT ID: NCT06207994 Recruiting - Clinical trials for Very Low Birth Weight Infant

PRICO: OPTI Target Range

POSTR
Start date: February 20, 2024
Phase: N/A
Study type: Interventional

The aim of the study is to determine if a narrower SpO2 Target Range setting automated control of FiO2 (A-FiO2) is more effective than a wider SpO2 Target Range

NCT ID: NCT06198478 Completed - Preterm Birth Clinical Trials

Tandem: Skin-to-skin Transfer From the Delivery Room to the Neonatal Unit

Tandem
Start date: March 3, 2017
Phase:
Study type: Observational

Immediate skin-to-skin contact (SSC) is already standard care for healthy term newborns, but its use for term or preterm newborns requiring admission to neonatal unit (NICU) with or without respiratory support is challenging. This study aimed to assess the safety and feasibility of SSC during the transfer of newborn infants, using a new purpose-built mobile shuttle care-station, called "Tandem". A monocentric prospective observational study was conducted at the tertiary referral center of the Université libre de Bruxelles in Brussels, Belgium Infants born with a birth weight above 1500g were eligible. Following initial stabilization, infants were placed in SSC with one of their parents and transferred to the NICU using the Tandem.

NCT ID: NCT06171867 Completed - Clinical trials for Neonatal Respiratory Distress

PNEUMACRIT Device for Neonatal Cardio Respiratory Monitoring

PNEUMACRIT
Start date: November 24, 2023
Phase: N/A
Study type: Interventional

The usability of a new PNEUMACRIT system is studied in clinical environment in this feasibility study.

NCT ID: NCT05737095 Recruiting - Preterm Birth Clinical Trials

Study of the Feasibility of Early Lung Ultrasound in Neonatal Respiratory Distress in Premature Newborns Born Between 32 Weeks of Amenorrhea and 36 Weeks Plus 6 Days of Amenorrhea, Hospitalized in the Neonatal Pediatrics and Intensive Care Units of the Dijon University Hospital

REchoPP
Start date: November 27, 2022
Phase:
Study type: Observational

Monocentric study carried out in the Neonatal and Intensive Care Units of the Dijon University Hospital. The objective is to evaluate the feasibility of performing a pulmonary ultrasound within 6 hours after admission in premature infants born between 32 weeks of amenorrhea and 36 weeks of amenorrhea + 6 days who are hospitalized for initial respiratory distress. Pulmonary ultrasound is performed within 6 hours of admission and an ultrasound score is calculated according to the images observed. Continued management according to protocols without taking into account the ultrasound data. Follow-up of patients until discharge from hospital or D28 of life (whichever comes first)

NCT ID: NCT05274386 Recruiting - Clinical trials for Very Low Birth Weight Infant

Evaluation of the Impact of SpO2 Averaging Time on Performance of an Automatic FiO2 Control System: a Randomized Study

Start date: February 17, 2022
Phase: N/A
Study type: Interventional

The aim of the study is to determine the preferred oximeter averaging setting during automated control of FiO2 (A-FiO2) in infants receiving respiratory support and supplemental oxygen.

NCT ID: NCT05257499 Completed - Clinical trials for Neonatal Respiratory Distress

In-person Versus Online Debriefing in HBB

Start date: October 5, 2021
Phase: N/A
Study type: Interventional

The objective of this study is to assess the effectiveness of online formative feedback and debriefing on nursing and medical students enrolled in the HBB course in comparison to traditional face-to-face feedback. The working hypothesis is that online feedback and debriefing during hands-on training sessions are as effective as face-to-face feedback and debriefing in teaching clinical skills to medical and nursing students.