The ARISE Study - Use of Vertical Positioning
ConditionAcute Respiratory Distress Syndrome
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUniversity of Alabama at Birmingham
About this trial
The pilot study will randomize 40 ARDS patients who if proning were required would be randomized to upright bed positioning or to stand of care with bed in the head of bed elevation position
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
Cancer
Active tracheostomy
Trial design
Design model
Parallel
Treatments tested in this trial
Intervention Upright Bed positioning
Other interventionPatient in receipt of the upright bed positioning will receive daily upright bed positioning time each day of mechanical ventilation following the time required by institutional protocol for ARDS - associated prone positioning
Treatment groups
40 Participants
are divided into 2 treatment groupsGroup A: InterventionActive comparator 1 intervention
Group B: Standard of CareNo intervention 0 interventions
Trial outcomes
Primary outcomes
1
Change in Tidal Volume
Mechanical Ventilator Tidal Volume
Time frame
within first 7 days of mechanical ventilationSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov