Clinical Trials Logo

RDS clinical trials

View clinical trials related to RDS.

Filter by:

NCT ID: NCT05493527 Recruiting - Clinical trials for Respiratory Tract Diseases

Noninvasive High Frequency Oscillatory Ventilation as a Post-extubation Respiratory Support in Neonates

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

A randomized controlled trial comparing Noninvasive high frequency oscillatory ventilation (NHFOV) and Noninvasive positive pressure ventilation (NIPPV) as post-extubation respiratory support in preterm neonates with respiratory distress syndrome(RDS)

NCT ID: NCT04820101 Not yet recruiting - RDS Clinical Trials

Dexmedetomidine for LISA Procedure in Preterm Infants

DEXLISA
Start date: May 15, 2021
Phase: N/A
Study type: Interventional

The investigators aim to evaluate: the effectiveness of dexmedetomidine for analgesia and sedation during LISA procedure, without compromising the respiratory drive; the safety of this drug on the preterm infant in a pilot study.

NCT ID: NCT03217162 Recruiting - ARDS Clinical Trials

Surfactant for Neonate With Acute Respiratory Distress Syndrome (ARDS)

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Acute respiratory distress syndrome (ARDS) in neonates has been defined, the role of surfactant is not clear. This study aimed to determine whether ARDS neonate would benefit from surfactant when oxygenation deteriorated on mechanical ventilation and to identify any potential risk factors related to mortality.

NCT ID: NCT03008200 Completed - RDS Clinical Trials

Fetal Pulmonary Artery Acceleration to Ejection Time Ratio (PATET) in the Prediction of Subsequent Development of Respiratory Distress Syndrome (RDS)

Start date: December 2015
Phase: N/A
Study type: Observational

Fetal PATET ratio evaluation to predict neonatal RDS

NCT ID: NCT02571231 Not yet recruiting - Clinical trials for Pulmonary Hypertension

High Flow Ventilation With Volume Guarantee

Start date: November 2015
Phase: N/A
Study type: Interventional

The trial is a pilot study performed in the NICU's at Oslo University Hospital and Haukeland University Hospital preparing a multi-center randomized, controlled unblinded cross-over study, comparing high frequency ventilation (HFV) with and without volume guarantee (VG).

NCT ID: NCT02076126 Completed - Premature Birth Clinical Trials

Determination of Lung Maturity and Prediction of RDS at Birth

Start date: March 2014
Phase: N/A
Study type: Observational

The overall objective is to identify quickly after birth the preterm infants who will develop respiratory distress syndrome (RDS) for the purpose of treating them as early as possible with surfactant, to reduce, and if possible, to avoid sequelae, including long-term oxygen treatment. We have therefore developed a quick test, which we believe will be ideal for this type of diagnostics, and will now test the method in a preclinical trial.

NCT ID: NCT01942473 Completed - Preterm Infant Clinical Trials

Effects of Automated Adjustment of FiO2 on Cerebral and Arterial Oxygenation in Preterm Infants

FiO2-Contr
Start date: August 2012
Phase: N/A
Study type: Interventional

In this study the investigators test the hypothesis that automated FiO2 adjustment increases the time of brain tissue oxygenation within the intended reference range. Furthermore, the investigators studied the change in workload during automated FiO2 adjustment as compared to manual adjustment by the nursing staff.

NCT ID: NCT01517958 Completed - Clinical trials for Respiratory Distress Syndrome

Lung Ultrasound to Diagnose Transient Tachypnea of the Newborn (TTN) Versus Respiratory Distress Syndrome (RDS) in Neonates

Start date: October 2011
Phase: N/A
Study type: Observational

The investigators hypothesize that ultrasonography of the newborn lung can be used as an effective diagnostic tool in neonates ≥ 28 weeks gestation with early symptoms of respiratory distress.

NCT ID: NCT01511952 Completed - Sepsis Clinical Trials

A Multi-Site Study of Music Therapy Interventions on Vitals, Feeding and Sleep in Premature Infants

Start date: January 2007
Phase: N/A
Study type: Interventional

This is a multi-site study of 272 premature infants >32 weeks who served in a randomized investigation (in morning or afternoon) where they served as their own controls. The infants' HR, RR, O2sats were measured with and without the implementation fo live music. The live interventions included songs of kin, selected by parents, the gato box and ocean disc played through entrained methods by a music therapist. The infants were evaluated within a two week period and in total each day including feeds, voids, activity level and sleep.

NCT ID: NCT01265589 Not yet recruiting - Infant, Newborn Clinical Trials

Intratracheal Vitamin A Administration With Surfactant for Newborn Respiratory Distress Syndrome

RDS
Start date: January 2012
Phase: Phase 3
Study type: Interventional

To research the effect of vitamin A to newborn respiratory distress syndrome by intratracheal administration with surfactant.