Intubation confirmation in newborns with volumetric device compared to the clinical method

Category Primary study
Registry of TrialsBrazilian Registry of Clinical Trials
Year 2016
INTERVENTION: Device E02.041.500 Will be evaluated the use of a volumetric device compared to the clinical method of confirmation endotracheal intubation in newborns The device remains connected to the tube until it is detected inflate or deflate the balloon or a maximum of 10 seconds. Then clinical confirmation is always performed The confirmation by the clinical method is the time of self inflatable balloon coupling to claim professional after his clinical evaluation of the confirmation of intubation There will be 20 participants in each group. A researcher will carry out the intervention while the other film the procedure CONDITION: C08.618.846 C23.300.707.500 E02.585 P00‐P96 respiratory failure, diaphragmatic hernia, intubation in neonates, confirm intubation ; E02.585 ; C08.618.846 ; C23.300.707.500 PRIMARY OUTCOME: Success rate for confirmation of endotracheal intubation by pedflow volumetric device and the clinical method; By pedflow balloon mobilization is evaluated after sealing of the two side orifices in a maximum time of 10 seconds; The clinical method confirmation will be made soon after the placement of self inflatable balloon on tracheal tube and evaluation movement of the chest wall, auscultation of axillary sounds and epigastric, pipe condensation in the exhalation, good ribcage expansion, increased oxygen saturation and heart rate SECONDARY OUTCOME: time will be evaluated to confirm the volumetric intubation device and also the clinical method, comparing the time required for each method ; INCLUSION CRITERIA: newborns that in selected hospitals requiring intubation in presence one of the researchers
Epistemonikos ID: 40508e3e492006e3b4c52417df433dccf320ee50
First added on: Aug 24, 2024