Intra Arrest Ventilation in Human Cadavers II
ConditionVentilation During Resuscitation
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMuehlenkreiskliniken, MKK
About this trial
The study investigates the influence of three types of ventilation mode by using Bi-Level positive airway pressure (pinsp 20 mbar, PEEP 5, AF 10/min) with two different types of ventilators ( Medumat vs. MeduVENT ), Continuous positive airway pressure (PEEP 5, AF 10/min, ASB 10) and Chest Compression Synchronized Ventilation (pInsp = 30 vs. 60 mbar; respiratory rate = chest compression rate, PEEP 5) with regard to achieving a sufficient tidal volume and the tightness of various supraglottic airway devices (laryngeal mask, i-Gel-laryngeal mask, laryngeal tube) and endotracheal intubation.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
more than 18 years of age
Disqualifiers
Adult respiratory distress syndrome (ARDS)
Severe lung or thoracic injuries
Pneumothorax
Abnormal airways
Trial design
Design model
Crossover
Treatments tested in this trial
treatment
Other intervention* Endotracheal Tube Ventilation with an endotracheal tub * Laryngeal tube Ventilation with a laryngeal tube * Laryngeal mask Ventilation with a laryngeal mask * I-Gel-Laryngeal Mask Ventilation with an I-Gel-laryngeal mask
Treatment groups
3 Participants
are divided into 3 treatment groupsGroup A: BIPAP (Bi-Level positive airway pressure)Active comparator 1 intervention
Group B: CPAP ASB (continouos positive airway pressure with assisted spontaneous breathing)Active comparator 1 intervention
Group C: CCSV (Chest Compression Synchronized Ventilation)Active comparator 1 intervention
Trial outcomes
Primary outcomes
1
gained tidalvolume with different airway devices in BIPAP
mean expiratory volume compared to ideal tidalvolume gained by using different airway devices in BIPAP
Time frame
After beginning of ventilation up to 4 minutes each device2
gained ventilation volume with different airway devices in CPAP-ASB
mean ventilation volume compared to ideal ventilation volume gained by using different airway devices in CPAP-ASB
Time frame
After beginning of ventilation up to 4 minutes each device3
occurred ventilation pressure with different airway devices in CCSV
mean ventilation pressure needed to develope a sufficient tidalvolume by using different airway devices in CCSV
Time frame
After beginning of ventilation up to 4 minutes each deviceSecondary outcomes
1
Mean peak pressure
Mean peak pressure during ventilation
Time frame
After beginning of ventilation up to 4 minutes each device2
Inspiratory pressure
Inspiratory pressure during ventilation
Time frame
After beginning of ventilation up to 4 minutes each device3
Peak pressure
Peak pressure during ventilation
Time frame
After beginning of ventilation up to 4 minutes each device4
Leakage volume
Leakage volume during ventilation
Time frame
After beginning of ventilation up to 4 minutes each deviceLocations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
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