Condition: Acute Respiratory Failure · Acute Respiratory Distress Syndrome · Chronic Respiratory Failure · Sponsor: Başakşehir Çam & Sakura City Hospital
The study is a multicentric prospective randomised cross-over study. It evaluates the compatibility of patients with the device without altering the routine treatment applied. During this evaluation, either the clinician-adjusted values on the device or the standard pre-set values are used to obtain hourly and 30-minute PVA (Patient Ventilator Asynchrony) recordings. These recordings will be analysed offline to identify the settings used and to compare the hourly and 30-minute PVA (Patient Ventilator Asynchrony) values when synchronisation is automatically set. The relationships and differences between these values will be analysed. For this purpose, the IntelliSync+ option, already available on the device, will be used. This software continuously analyses waveform signals at least a hundred times per second. This allows for the immediate detection of patient efforts and the initiation of inspiration and expiration in real time, thereby replacing traditional trigger settings for inspiration and expiration. If the patient is already synchronised with this option, it will then be possible to switch to traditional synchronisation settings for comparison. Statistical analyses will be conducted using SPSS 24.0, JASP (Just Another Statistical Programme), Jamovi ( fork of JASP), or R software. Initially, all numerical and categorical data will be evaluated using descriptive statistical methods. The distributions of numerical variables will be examined using visual (histograms and pr…
This description comes directly from the study's public registry record.
Ramazan Guven, Associate professor · 05324935995 · drramazanguven@gmail.com
Tuba Dogan, MD · dr.tubadogan@hotmail.com
Always discuss trial participation with your own doctor first.
| Dr.Suat Seren Chest Diseasees Hospital | Izmir, Turkey (Türkiye) | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06357780