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NCT Number: NCT06254456

Fluid Responsiveness in Prone Patients

To assess fluid responsiveness in prone patient

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Key information

Conditions

Fluid Responsiveness

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

End expiratory occlusion test

Diagnostic Test

Fluid responsiveness test

Other names: Tidal volume challenges test

Primary outcomes

  1. Pulse Pressure Variation

    Time frame: 1 year

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

Sponsors and collaborators

Lead sponsor

Bhumibol Adulyadej Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2025
Study completion
2028
First posted
Feb 12, 2024
Registry last updated
Feb 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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