Respiratory Distress Syndrome, Newborn Clinical Trial
Official title:
Effect of Position on the Spontaneous Breathing Trial
Verified date | February 2018 |
Source | Christiana Care Health Services |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Mechanical ventilation is a life-sustaining intervention in premature infants with
respiratory difficulties. There is relative consensus when to intubate and provide positive
pressure mechanical ventilation in the presence of respiratory failure. In contrast,
discontinuation of mechanical ventilation during recovery remains largely subjective. A
potential predictive tool for neonatal extubation is the Spontaneous Breathing Trial (SBT).
The efficacy of SBT or other tests used in older patient populations in improving clinical
judgment is questionable in the neonatal population with its unique physiology, respiratory
mechanics and drive factors. Christiana Care Health System NICU currently uses the SBT as a
standard part of neonatal assessment for extubation from mechanical ventilation.
Infants in the CCHS NICU are routinely cared for in multiple positions (prone, supine,
lateral) throughout the day. What is unknown is the impact of infant positioning on the SBT.
An SBT performed in one position may not predict infant respiratory status after extubation
in another position. Understanding the impact of infant positioning and work of breathing
indices independently or in combination with an SBT will aid clinicians in decision-making
and potentially decrease neonatal morbidity (inaccuracy with timing and safety of
extubation). This pilot study will begin to explore these clinically relevant factors.
Objectives: This pilot study will investigate the (1) role of infant position on SBT score
and (2) the relationship of work of breathing indices in reference to the SBT score and
infant position.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | September 2018 |
Est. primary completion date | July 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 24 Weeks to 34 Weeks |
Eligibility |
Inclusion Criteria: - Infants born 24+0 to 34+6 weeks gestation - Intubated for a minimum of 24hrs - Qualify for an SBT as standard of care. Exclusion Criteria: - Previous history of abdominal or chest surgery - Congenital malformation of the chest or abdomen - Neuromuscular disorder - Current medications affecting neuro-muscular tone - Unable to be positioned either prone, supine or lateral as determined by the attending neonatologist. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Christiana Care Health Services |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Impact of infant positioning on spontaneous breathing test (SBT) pass rates | SBT will be performed with the infant in 3 different positions (supine, prone, side-lying). | Less than 1 hour | |
Primary | Impact of infant positioning on spontaneous breathing test (SBT) fail rates | SBT will be performed with the infant in 3 different positions (supine, prone, side-lying) | Less than 1 hour | |
Secondary | WOB correlates of SBT pass rates | Pulmonary function tests will be performed during the SBT in each position (supine, prone and side-lying). | Less than 1 hour | |
Secondary | WOB correlates of SBT fail rates | Pulmonary function tests will be performed during the SBT in each position (supine, prone and side-lying). | Less than 1 hour |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT01206946 -
Efficacy of Antenatal Steroids in Reducing Respiratory Morbidities in Late Preterm Infants
|
Phase 2 | |
Completed |
NCT00739115 -
The Use of Heliox Via Nasal CPAP to Prevent Early CPAP Failure in Premature Infants: A Feasibility Study
|
N/A | |
Terminated |
NCT00486395 -
Will CPAP Reduce Length Of Respiratory Support In Premature Infants?
|
Phase 3 | |
Completed |
NCT01242462 -
Feasibility of Mid-frequency Ventilation in Newborns With RDS: Randomized Crossover Pilot Trial
|
Phase 1/Phase 2 | |
Enrolling by invitation |
NCT02050971 -
Autologous Cord Blood Infusion for the Prevention and Treatment of Prematurity Complications In Preterm Neonates
|
Phase 1 | |
Completed |
NCT00486850 -
Synchronized Intermittent Mandatory Ventilation (SIMV) Versus Nasal Intermittent Positive Pressure Ventilation (NIPPV) In Preterm Infants With Respiratory Distress
|
Phase 4 | |
Terminated |
NCT00005776 -
Inhaled Nitric Oxide Study for Respiratory Failure in Newborns
|
Phase 3 | |
Completed |
NCT04500353 -
Routine Or Selective Application of a Face Mask for Preterm Infants at Birth: the ROSA Trial
|
N/A | |
Completed |
NCT05796128 -
NIPPV vs.nCPAP During LISA Procedure
|
N/A | |
Terminated |
NCT01467076 -
Inhaled Prostaglandin E1 (IPGE1) for Hypoxemic Respiratory Failure (NHRF)
|
Phase 2 | |
Completed |
NCT00828243 -
Genetic Regulation of Surfactant Deficiency
|
||
Completed |
NCT00556738 -
Intrapulmonary Percussive Ventilation (IPV) Versus Nasal Continuous Positive Airway Pressure Ventilation (nCPAP) in Transient Respiratory Distress of the Newborn
|
N/A | |
Not yet recruiting |
NCT05594030 -
Thoracic Fluid Content by Electric Bioimpedance Versus Lung Ultrasound in Preterm Neonates With Respiratory Distress
|
||
Completed |
NCT02332304 -
Amniotic Fluid Optical Density Determination as a Test for Assessment of Fetal Lung Maturity.
|
Phase 3 | |
Withdrawn |
NCT00598429 -
Inhaled PGE1 in Neonatal Hypoxemic Respiratory Failure
|
Phase 2 | |
Completed |
NCT04137783 -
ABCA3 Gene and RDS in Late Preterm and Term Infants
|
||
Completed |
NCT01941524 -
Brain Oxygenation and Function of Preterm Newborns During Administration of Two Different Surfactant Preparations
|
Phase 4 | |
Completed |
NCT01102543 -
Observational Study on the Prophylactic Use of Curosurf in Neonatal Respiratory Distress Syndrome (RDS)
|
N/A | |
Completed |
NCT00501982 -
Efficacy of Combining Prophylactic Curosurf With Early Nasal CPAP in Delivery Room: the Curpap Study
|
Phase 4 | |
Recruiting |
NCT05065424 -
Premedication for Less Invasive Surfactant Administration Study (PRELISA)
|
Phase 4 |