Neonatal Respiratory Failure

3

Review clinical trials related to Neonatal Respiratory Failure. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Dexmedetomidine for Invasive Ventilation In the NEOnate

Despite the increasing use of non-invasive ventilation, a large majority of premature neonates still receive invasive ventilation during their NICU (neonatal intensive care unit) stay. Invasive ventilation is a unanimous source of discomfort and pain. As opposed to the adult and pediatric population, routine use of opioids or midazolam is not recommended in ventilated neonates. Although opioids are the most frequently prescribed analgosedative drugs in ventilated premature neonates, their use is controversial because of the risk of respiratory depression - which can prolong invasive ventilation- and concerns on long-term neurodevelopment. Dexmedetomidine, a selective alpha-2- adrenergic agonist routinely used in the adult ICU (intensive care unit), provides light sedation and some analgesia with no or little respiratory-depression effect. It also has neuroprotective properties after pediatric cardiac surgery and in neonatal animal models. Dexmedetomidine is thus a promising candidate drug in ventilated premature neonates that might reduce the duration of mechanical ventilation and preserve neurodevelopment in this vulnerable population. The investigators hypothesize that the use of dexmedetomidine in ventilated premature neonates could decrease the need for opioids, facilitate extubation and thereby preserve long-term neurodevelopmental outcome.

Participants needed: 246
Trial details
Phase: Phase 2, Phase 3Age: Up to 10Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Intercommunal CreteilUpdated: Mar 25, 2026Locations: 12
Eligibility criteria

Neonates with a gestational age at birth < 32 weeks of gestation and corrected g... [+4]

Previous inclusion in this trial [+9]

Status: Not yet recruiting

Lung Ultrasound-Guided Respiratory Management in Infants

This single-center randomized controlled study will compare lung ultrasound-guided respiratory management with standard clinical care in infants requiring respiratory support. The primary outcome measure is length of NICU stay.

Participants needed: 64
Trial details
Age: 0-1Biological sex: AllType: InterventionalSponsor: Tufts Medical CenterUpdated: Feb 4, 2026
Eligibility criteria

Infants admitted to the Tufts Medical Center NICU [+3]

Major congenital anomalies [+4]

Status: Recruiting

Flow and Grow - The Ideal Time to Wean CPAP Off In Extremely Low Birth Weight Infants

Preterm neonates born at less than 30 weeks' gestation are commonly maintained on invasive or non-invasive respiratory support to facilitate gas exchange. While non-invasive respiratory support (NIS) can be gradually reduced over time as the infant grows, most weaning strategies often lead to weaning failure. This failure is evidenced by an increase in significant events such as apneas, desaturations, and/or bradycardias, increased work of breathing, or an inability to oxygenate or ventilate, resulting in escalated respiratory support. Although the optimal approach to weaning NIS remains uncertain, neonatal units that delay Continuous Positive Airway Pressure (CPAP) weaning until 32-34 weeks corrected gestational age exhibit lower rates of chronic lung disease. Therefore, the investigators aim to compare the duration on respiratory support and oxygen exposure in infants born at less than 30 weeks' gestational age who undergo a structured weaning protocol that includes remaining on CPAP until at least 32-34 weeks corrected gestational age (CGA). The hypothesis posits that preterm infants following a structured weaning protocol, including maintaining CPAP until a specific gestational age, will demonstrate lower rates of weaning failure off CPAP (defined as requiring more support and/or experiencing increased stimulation events 72 hours after CPAP weaning) than those managed according to the medical team's discretion.

Participants needed: 130
Trial details
Age: Up to 30Biological sex: AllType: InterventionalSponsor: University of California, San DiegoUpdated: Jan 20, 2026Locations: 5
Eligibility criteria

All infants admitted to the NICU at Jacobs, Rancho Springs, Scripps La Jolla, Ra... [+1]

Declined or unable to give informed consent [+2]