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IRCT2016080825732N8 IRCT 2017-01-16 Semnan University of Medical Sciences, Vice Chancellor for Research and Technology comparison of therapeutic effect of surfactant injection through tracheal in neonates with respiratory distress syndrome hospitalized in Amir al-momenin Hospital in Semnan comparison of surfactant injection through tracheal in neonates with respiratory distress syndrome 2016-03-20 anticipated 200 Complete https://irct.ir/trial/21484 interventional Randomization: Not randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment. N/A Respiratory distress syndrome. Intervention 1: Intervention group: Surfactant injection (Prescribed according to the instructions the manufacturer and section stock) to method of INSURE for all neonates with respiratory distress syndrome (RDS) hospitalized in the neonatal intensive care unit Amiralmomenin hospital, Semnan. Intervention 2: In control group, no intervention was performed and were assessed only for comparison of two groups of the study.
public Dr Shamsollah Nouripour
Amiralmomenin Hospital, Blvd Mostafa Khomeini, Semnan
Semnan Iran (Islamic Republic of) +98 23 3345 1336 are20935@gmail.com Semnan University of Medical Sciences scientific Dr Shamsollah Nouripour
Amiralmomenin Hospital, Blvd Mostafa Khomeini, Semnan
Semnan Iran (Islamic Republic of) +98 23 3345 1336 are20935@gmail.com Semnan University of Medical Sciences Iran (Islamic Republic of) Inclusion criteria: premature infants admitted to the neonatal intensive care unit with definitive diagnosis of RDS by pediatrician using clinical symtoms including tachypnea, intercostal retraction, nasal flaring, cyanosis, and hypotension and respiratory arrest. Exclusion criteria: infants with major abnormalities, chromosomal abnormalities, severe asphyxia, and need to Antvbyshn at birth. 1 day 1 day Both P22.0 Respiratory distress syndrome of newborn Treatment - Drugs Treatment - Drugs Intervention group: Surfactant injection (Prescribed according to the instructions the manufacturer and section stock) to method of INSURE for all neonates with respiratory distress syndrome (RDS) hospitalized in the neonatal intensive care unit Amiralmomenin hospital, Semnan. In control group, no intervention was performed and were assessed only for comparison of two groups of the study. Severity of respiratory distress. Timepoint: Before starting study and one hour after Following Prescribing Dosing surfactant. Method of measurement: Based on radiography. Apgar score. Timepoint: minute one and five Birth. Method of measurement: View Information registered records Filed in the labor. Severity of respiratory distress. Timepoint: After injecting surfactant. Method of measurement: Based on Picture Radiography. Semnan University of Medical Sciences, Vice Chancellor for Research and Technology Approved 2016-05-25 Semnan University of Medical Sciences, Deputy of research and technology, Ethics Committee Semnan University of Medical Sciences, Basij Blvd, Semnan Semnan Iran (Islamic Republic of)