Status:
COMPLETED
Observational Study Evaluating the Use of Intellivent® for Patients With Respiratory Distress Syndrome
Lead Sponsor:
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Conditions:
Respiratory Distress Syndrome
Eligibility:
All Genders
18+ years
Brief Summary
Rational: Intellivent is a ventilation mode completely automated which controls ventilation and oxygenation parameters. Safety and performance of IntelliVent has still been demonstrated in post operat...
Eligibility Criteria
Inclusion
- Patient which needs an invasive ventilation
- Intubation \< 24 hours
- Age ≥ 18 years
Exclusion
- Patient which has withdrawal standard in line with the unit coming off procedure (all criteria must be present)
- temperature ≤ 38,5°C
- No pressor drug
- No sedation,
- Motor response to order,
- Cough during bronchoaspiration
- %VM ≤ 130%, FiO2 ≤ 50%, PEEP ≤ 5 cmH2O, Pinsp ≤ 25 cmH2O.
- Patient with non invasive ventilation .
- Dysfunctions of the ventilatory command (ex Cheyne-Stokes).
- Broncho pleural fistula.
- Brain dead status.
- Pregnant woman.
- Adult under guardianship.
- Person deprived of liberty
Key Trial Info
Start Date :
January 1 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 1 2013
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT01489085
Start Date
January 1 2013
End Date
April 1 2013
Last Update
July 22 2014
Active Locations (1)
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1
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Toulon, France, 83056