TCTR20220705008
Completed
Not Applicable
Sepsis-related Pediatric Acute Respiratory Distress Syndrome: A Multicenter Observational Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- pediatric acute respiratory distress syndrome
- Sponsor
- Ramathibodi Hospital
- Enrollment
- 132
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
Sepsis-related PARDS patients had more severe illness and higher morbidities and mortality than non-sepsis PARDS patients.
Investigators
Eligibility Criteria
Inclusion Criteria
- •The screened patients were children 1 month to 18 years old who required intubation during the study period
Exclusion Criteria
- •The exclusion criteria were premature neonates with a corrected age less than 35 weeks, PARDS established outside of our centers, congestive heart failure, or perinatal\-related lung disease
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Pediatric Acute Respiratory Distress Syndrome Asia StudyAcute Respiratory Distress SyndromePediatric Intensive Care UnitMechanical VentilationNCT04068038KK Women's and Children's Hospital738
Completed
Not Applicable
Pediatric Acute Respiratory Distress Syndrome Ventilation BundleAcute Respiratory Distress SyndromeNCT03504176KK Women's and Children's Hospital134
Terminated
Phase 4
Paediatric Ards Neuromuscular Blockade StudyARDSNCT02902055University Medical Center Groningen3
Completed
Not Applicable
Identifying PARDS EndotypesRespiratory Distress SyndromeRespiratory Distress Syndrome, AdultNCT03539783Children's Hospital Medical Center, Cincinnati76
Completed
Phase 2
Adverse Neonatal Outcomes with a Shortened Clinical Regimen of Dexamethasone.Preterm BirthDistress Respiratory SyndromeNCT06569251Ricardo A Gutierrez Ramirez, MD, MSc, FACOG68