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Respiratory Distress Syndrome clinical trials

View clinical trials related to Respiratory Distress Syndrome.

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NCT ID: NCT01664832 Recruiting - Clinical trials for Respiratory Distress Syndrome

Is Synchronization More Effective During Noninvasive Ventilation in Immediately Extubated Preterm Infants?

N_SIMV
Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of this study is the examination of the hypothesis that synchronized nasal IMV as compared to non-synchronized nasal IMV will decrease breathing effort in preterm infants immediately after extubation when recovering from Respiratory distress syndrome (RDS). Another objective is to examine the effects for synchronized non-invasive mechanical ventilation on gas exchange and cerebral oxygen saturation.

NCT ID: NCT01189162 Recruiting - Clinical trials for Respiratory Distress Syndrome

High Flow Nasal Cannula (HFNC) Versus Nasal Intermittent Mandatory Ventilation (NIMV)for Respiratory Distress Syndrome (RDS): a Randomized, Controlled, Prospective Study

Start date: January 2010
Phase: N/A
Study type: Interventional

The investigators hypothesize that while the extremely low birthweight (ELBW) infants (<1000 g) may need NIMV for the treatment of RDS, larger infants or the smaller ones post extubation may enjoy the comfort benefits associated with HFNC while getting coparable respiratory support to NIMV.

NCT ID: NCT00883532 Recruiting - Clinical trials for Respiratory Distress Syndrome

Prevention of Chronic Lung Disease (CLD) in Preterm Infants

Start date: April 2009
Phase: Phase 4
Study type: Interventional

Pulmonary inflammation plays an important role in the early development of CLD. Postnatal glucocorticoids have been shown effective in the prevention or treatment of CLD with various success. However, systemic glucocorticoid therapy often associated with various short term and long term complications. Therefore, modification of the therapeutic regimen is needed. Inhaled steroid, including inhaled budesonide,have been tried but the results are essentially unsuccessful, most likely due to small airways that the inhaled steroid reaching to the peripheral lungs are limited and unpredictable. Direct instillation of budesonide into the airway has also shown to be ineffective, possibly due to poor distribution of steroid in the lungs. The investigators hypothesize that intratracheal instillation of budesonide, a strong tropical steroid, using surfactant as vehicle would facilitate the delivery of budesonide to the lung periphery and would inhibit lung inflammation and improve the pulmonary outcome. The result of our pilot study (Pediatrics, 2008) indicated this high possibility.

NCT ID: NCT00368680 Recruiting - Clinical trials for Respiratory Distress Syndrome

Early CPAP in Respiratory Distress Syndrome

Start date: January 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to establish if a strategy of EBCPAP application in a subgroup of VLBWI, 800 to 1500g birthweight, decreases the need for mechanical ventilation in this group, without affecting mortality.

NCT ID: NCT00277030 Recruiting - Clinical trials for Respiratory Distress Syndrome

Two Strategies of RDS Treatment in Newborns With Birth Weight > 1500 Grams

Start date: January 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare two different treatment strategies for RDS in preterm infants > 1500 grams and evaluate whether a selective surfactant administration would reduce the need of intubation, mechanical ventilation and surfactant use.

NCT ID: NCT00006274 Recruiting - Clinical trials for Respiratory Distress Syndrome

Study of Energy Requirements in Critically Ill Newborns

Start date: March 1997
Phase: N/A
Study type: Observational

OBJECTIVES: I. Determine the total energy expenditure in term and preterm infants in both well and ill states using the doubly labeled water method.