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Evaluation of Corrected Carotid Artery Flow Time as a Predictor of Fluid Responsiveness in Spontaneous Breathing Patients

Completed
Conditions
Brain Tumor
Interventions
Device: ultrasonographic measurement of corrected flow time in carotid artery
Registration Number
NCT02843477
Lead Sponsor
Yonsei University
Brief Summary

It is still challenging to assess intravascular volume status in spontaneously breathing patients. Recently, the measurement of corrected flow time in carotid artery was introduced as quite useful, simple and noninvasive for the evaluation of circulating blood volume change. The aim of this study is to evaluate whether corrected carotid artery flow time as determined by ultrasonography can be a predictor of fluid responsiveness in spontaneously breathing patients before induction of general anesthesia.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • adult patients (19-80 years of age) who were scheduled to undergo elective neurosurgery for brain tumor
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Exclusion Criteria
  • BMI > 35 or < 15 kg/m2
  • the presence of carotid artery stenosis > 50%
  • systolic blood pressure > 160 mmHg
  • cardiac rhythm other than sinus
  • intracardiac shunt 6. valvular heart disease
  • a left ventricular ejection fraction of < 50%
  • right ventricular dysfunction 9
  • chronic obstructive pulmonary disease
  • pulmonary hypertension
  • chronic kidney disease (eGFR < 60 mL/min/1.73m2)
  • pregnancy
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Fluid loading groupultrasonographic measurement of corrected flow time in carotid arterySpontaneously breathing patients before induction of general anesthesia who receive fluid loading
Primary Outcome Measures
NameTimeMethod
ultrasonographic measurement of corrected flow time in carotid artery5 minutes after fluid loading

The ultrasonographic measurement of corrected flow time in carotid artery will be performed 5 minutes after fluid loading.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institue, Yonsei Universiy College of Medicine

🇰🇷

Seoul, Korea, Republic of

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