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Positive End-expiratory Pressure (PEEP) in Predicting Fluid Responsiveness in Patients Undergoing One-lung Ventilation

H

Hallym University Kangnam Sacred Heart Hospital

Status

Completed

Conditions

Lung Diseases
Lung Cancer

Treatments

Procedure: PEEP challenge

Study type

Interventional

Funder types

Other

Identifiers

NCT03794414
2018-11-028

Details and patient eligibility

About

The present study is to evaluate the effect of positive end-expiratory pressure (PEEP) in predicting fluid responsiveness in patients undergoing one-lung ventilation.

Full description

Appropriate fluid challenge is crucial during lung surgery under one-lung ventilation. Applying PEEP in mechanically ventilating patients changes dynamic hemodynamic parameters (stroke volume variation, pulse pressure variation), which is more pronounced in hypovolemic patients. The aim of the present study is to evaluate the mechanically ventilating patients under one-lung ventilation requiring fluid resuscitation by applying PEEP to predict fluid responsiveness.

The investigators hypothesized that applying PEEP in one-lung ventilating patients can also change dynamic parameters and the magnitude of the change of stroke volume variation, pulse pressure variation can predict fluid responsiveness. The investigator applied PEEP 10 mmHg in one-lung ventilating patients and observed the dynamic parameters including stroke volume variation, pulse pressure variation and then infused 6ml/kg of crystalloid for fluid challenge and diagnosed fluid responsiveness as 10% increase of stroke volume after fluid challenge.

Enrollment

40 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients undergoing lung surgery under one-lung ventilation

Exclusion criteria

  • arrhythmia
  • moderate to severe valvular heart disease moderate to severe pericardial effusion left ventricular ejection fraction < 40%
  • moderate to severe chronic obstructive lung disease
  • unable to insert oesophageal Doppler Monitor (ODM) probe ( esophageal stent, esophageal cancer, previous esophageal surgery, esophageal stricture, esophageal varices, pharyngeal pouch and severe coagulopathy )
  • patient refusal
  • cannot understand the protocol
  • less than 50kg or over 100kg in weight

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

fluid responder
Experimental group
Description:
patients with 10% or more increase in stroke volume after fluid challenge. Both arms receive PEEP challenge.
Treatment:
Procedure: PEEP challenge
fluid non-responder
Experimental group
Description:
patients with no increase or less than 10% increase in stroke volume after fluid challenge. Both arms receive PEEP challenge
Treatment:
Procedure: PEEP challenge

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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