Fluid Responsiveness in Prone Patients

End Expiratory Occlusion Test and Tidal Volume Challenge Test for Assess Fluid Responsiveness in Prone Patients

Status

Not yet recruiting

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06254456

Enrollment

Registered

2024-02-12

Start date

2024-03-01

Completion date

2028-07-04

Last updated

2024-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fluid Responsiveness

Keywords

Fluid responsiveness, prone, EEOT, TVC, ARDS

Brief summary

To assess fluid responsiveness in prone patient

Interventions

DIAGNOSTIC_TESTEnd expiratory occlusion test

Fluid responsiveness test

Study design

Allocation

Intervention model

SEQUENTIAL

Primary purpose

DIAGNOSTIC

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* patients planed to prone position for treatment

Exclusion criteria

* no consent * arrhythmia * pregnancy * pre existing pneumothorax * pre existing fluid overload * cannot insert arterial or central venous catheters

Design outcomes

Primary

Measure	Time frame	Description
Pulse Pressure Variation	1 year	Detect the pulse pressure variation from cardiac output monitoring ( A- line )

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026