Fluid Responsiveness in Prone Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBhumibol Adulyadej Hospital

About this trial

To assess fluid responsiveness in prone patient

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients planed to prone position for treatment

Disqualifiers

no consent

arrhythmia

pregnancy

pre existing pneumothorax

Trial design

Design model

Sequential

Treatments tested in this trial

  • End expiratory occlusion test

    Diagnostic test

    Fluid responsiveness test

Treatment groups

84 Participants
are divided into 1 treatment group
Group A: Prone patientsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pulse Pressure Variation

Detect the pulse pressure variation from cardiac output monitoring ( A- line )

Time frame
1 year

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: