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Sedation Patient Articles & Analysis

9 news found

Belgian scale-up Oncomfort raises €10 million in Series A funding co-led by Debiopharm and Crédit Mutuel Innovation

Belgian scale-up Oncomfort raises €10 million in Series A funding co-led by Debiopharm and Crédit Mutuel Innovation

Oncomfort, the Belgian inventor of and leader in Digital Sedation - a new method for relieving patients’ pain and anxiety without medication - today announces the completion of a €10 million Series A funding round co-led by two prominent institutional investors: Debiopharm and Crédit Mutuel Innovation. ...

ByOncomfort


Co-creative Innovation with BioWin

Co-creative Innovation with BioWin

In 2017, Oncomfort created a medical device for Digital Sedation™, a digital therapeutic alternative to pharmacological sedation. More than 80.000 patients have already been treated with Digital Sedation™ in regular practice, demonstrating the feasibility and validity of delivering sedation during ...

ByOncomfort


Oncomfort receives ISO 13485:2016 certification

Oncomfort receives ISO 13485:2016 certification

ncomfort, the leader in Digital Sedation™, a digital therapy to relieve patient anxiety and pain, today announces that it has obtained the ISO 13485:2016 certification by certification company DARE!! ...

ByOncomfort


Liberate Medical Reports Positive Pilot Trial Results of VentFree Respiratory Muscle Stimulator

Liberate Medical Reports Positive Pilot Trial Results of VentFree Respiratory Muscle Stimulator

Applying non-invasive electrical stimulation to the expiratory abdominal muscles may reduce abdominal muscle atrophy and markedly reduce the number of days adult patients require mechanical ventilation – a potentially important finding for weaning ventilated patients, including seriously ill COVID-19 patients, and improving patient outcomes. Liberate Medical today announced the results of ...

ByLiberate Medical, LLC


VentFree Respiratory Muscle Stimulator receives FDA Emergency Use Authorization for Use During COVID-19 Pandemic

VentFree Respiratory Muscle Stimulator receives FDA Emergency Use Authorization for Use During COVID-19 Pandemic

Liberate Medical today announced that it has received Federal Drug Administration (FDA) Emergency Use Authorization for its VentFree™ Respiratory Muscle Stimulator, intended to be used to reduce disuse atrophy of the abdominal wall muscles, which may reduce the number of days adult patients require mechanical ventilation, including those patients with ...

ByLiberate Medical, LLC


Check-Cap Announces Positive Results from U.S. Pilot Study of C-Scan System

Check-Cap Announces Positive Results from U.S. Pilot Study of C-Scan System

No device or procedure related serious adverse events (SAEs) were reported and all device or procedure related adverse events were mild in severity. In total, 45 patients enrolled in the study, of which 40 patients underwent the study procedure. ...

ByCheck-Cap Ltd.


Liberate Medical Announces CE Marking for its VentFree Respiratory Muscle Stimulator

Liberate Medical Announces CE Marking for its VentFree Respiratory Muscle Stimulator

VentFree is intended to prevent abdominal muscle atrophy and reduce ventilation duration in mechanically ventilated patients. Liberate published the results of its pilot trial of VentFree in July, which found a shorter ventilation duration and ICU length of stay in patients who received VentFree compared with standard of care. ...

ByLiberate Medical, LLC


Liberate Medical Presents Data from its Pilot Trial of VentFree, a Muscle Stimulator for Mechanically Ventilated Patients, at the American Thoracic Society 2019 International Conference

Liberate Medical Presents Data from its Pilot Trial of VentFree, a Muscle Stimulator for Mechanically Ventilated Patients, at the American Thoracic Society 2019 International Conference

“The results from this successful pilot study support our belief that VentFree has the potential to save lives, reduce morbidity and significantly decrease hospital costs for these patients.” About Prolonged Mechanical Ventilation Approximately 40% of patients who need mechanical ventilation need it for more than four days, and the number of these ...

ByLiberate Medical, LLC


Liberate Medical’s VentFree Muscle Stimulator Receives Breakthrough Device Designation from the FDA to Reduce Mechanical Ventilation Duration

Liberate Medical’s VentFree Muscle Stimulator Receives Breakthrough Device Designation from the FDA to Reduce Mechanical Ventilation Duration

” About Prolonged Mechanical Ventilation Approximately 40% of mechanically ventilated patients require more than four days of ventilator support, and the number of these patients is increasing at 5.5% per year. ...

ByLiberate Medical, LLC

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