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Bronchiolitis clinical trials

View clinical trials related to Bronchiolitis.

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NCT ID: NCT06204367 Enrolling by invitation - Bronchiolitis Clinical Trials

Evaluation of Lung Ultrasonography Findings in Newborns With Respiratory Syncytial Virus Bronchiolitis

Start date: December 1, 2023
Phase:
Study type: Observational [Patient Registry]

Respiratory Syncytial Virus (RSV) is a seasonal, highly contagious pathogen belonging to the Pneumoviridae (genus orthopneumovirus), a family of negative-strand RNA viruses. Lung ultrasonography; Today, it has become frequently used in neonatal intensive care units because it is a diagnostic, useful, harmless, radiation-free, bedside, reproducible and practical method. The primary purpose of the study is to record lung ultrasound findings and score and thus to compare the agreement between lung ultrasonography and clinical score in the diagnosis and follow-up of newborn babies who are followed up in the neonatal intensive care unit due to bronchiolitis caused by RSV and other viral factors, which are frequently encountered.

NCT ID: NCT04039347 Enrolling by invitation - Clinical trials for Bronchiolitis Obliterans

Extension Trial on Efficacy / Safety of L-CsA + SoC in Treating BOS in Post Single or Double Lung Transplant (BOSTON-3)

BOSTON-3
Start date: March 12, 2020
Phase: Phase 3
Study type: Interventional

The objective of the trial is to assess the long-term safety and efficacy of L-CsA plus Standard of Care (SoC) in the treatment of BOS in single (SLT) and double lung transplant (DLT) recipients.

NCT ID: NCT03345628 Enrolling by invitation - Pneumonia Clinical Trials

Feasibility Study for Neurodevelopment Follow-up Study in PICU

PICUFUN
Start date: February 1, 2018
Phase:
Study type: Observational

There is a large and growing body of animal evidence demonstrating neuroapoptosis and neurodevelopmental abnormalities after exposure to anesthetic agents. This has prompted an FDA warning concerning use of anesthetics and sedatives in children under 3 years of age. There has been very little investigation of the neurodevelopment effects of prolonged sedation in previously healthy infants in Paediatric Intensive Care. This feasibility study will recruit previously healthy infants who required respiratory support with or without sedation at up to 1 year of age and assess neurodevelopmental outcomes at 6 years of age.