Not yet recruiting NCT06254456
Fluid Responsiveness in Prone Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: End expiratory occlusion test.
- Who it may be relevant to
- Registry conditions: Fluid Responsiveness. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
End Expiratory Occlusion Test and Tidal Volume Challenge Test for Assess Fluid Responsiveness in Prone Patients
Overview
To assess fluid responsiveness in prone patient
Interventions
- Diagnostic test End expiratory occlusion test
Fluid responsiveness test
Primary outcome measures
- Pulse Pressure Variation [Time frame: 1 year]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Sequential
- Masking
- Open label
- Primary purpose
- Diagnostic
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06254456 · 95/66