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NCT06254456 Clinical Trial

Fluid Responsiveness in Prone Patients

Fluid Responsiveness Clinical Trial

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06254456
Other study ID # 95/66
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 1, 2024
Est. completion date July 4, 2028

Study information
Verified date February 2024
Source Bhumibol Adulyadej Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess fluid responsiveness in prone patient

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 84
Est. completion date July 4, 2028
Est. primary completion date May 4, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• End expiratory occlusion test
Fluid responsiveness test

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Bhumibol Adulyadej Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary Pulse Pressure Variation Detect the pulse pressure variation from cardiac output monitoring ( A- line ) 1 year
See also
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Withdrawn NCT01898975 - A Gray Zone Approach to Stroke Volume Variation Derived From NICOM N/A
Completed NCT05419570 - Short Time Low PEEP Challenge and Mini Fluid Challenge