Skip to main content
Clinical Trials/NCT06733389
NCT06733389
Not yet recruiting
Not Applicable

Comparison of Peripheral Venous Pressure Variation, Pulse Pressure Variation and Pleth Variability Index in Predicting Fluid Responsiveness

Seoul National University Bundang Hospital1 site in 1 country150 target enrollmentDecember 28, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pulse Pressure Variation
Sponsor
Seoul National University Bundang Hospital
Enrollment
150
Locations
1
Primary Endpoint
Fluid responsiveness
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

Pulse pressure variation (PPV) and pleth variability index (PVI) are widely used in clinical practice as indicators of the responsiveness to fluid therapy in patients receiving mechanical ventilation. PPV, which measures changes in arterial pressure, requires arterial puncture, which is invasive, and PVI, which detects subtle changes in oxygen saturation, requires an expensive, commercial monitoring equipment. In this study, we aimed to measure peripheral venous pressure variation using less invasive waveform variation in peripheral veins and to determine whether this indicator can be clinically used to predict the responsiveness to fluid therapy. In addition, the investigators aimed to confirm the superiority of the indicators by comparing them with the responsiveness to fluid therapy of the PPV and PVI.

Detailed Description

Pulse pressure variation (PPV) and pleth variability index (PVI) are widely used in clinical practice as indicators of the responsiveness to fluid therapy. The investigators aimed to measure peripheral venous pressure variation using less invasive waveform variation in peripheral veins and to determine whether this indicator can be clinically used to predict the responsiveness to fluid therapy.

Registry
clinicaltrials.gov
Start Date
December 28, 2024
End Date
November 28, 2026
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Park InSun

Principal investigator

Seoul National University Bundang Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients voluntarily agreed and signed the written informed consent form before participating in the study
  • Adults aged 19 years or older
  • American Society of Anesthesiologists physical class (ASA) 1-3
  • Patients scheduled for elective hepatectomy under general anesthesia
  • Patients who require arterial pressure monitoring and additional peripheral venous access for routine anesthesia preparation
  • Non-smokers with normal pulmonary function

Exclusion Criteria

  • Patients with abnormal findings on electrocardiogram before surgery
  • Patients who cannot undergo peripheral venous puncture

Outcomes

Primary Outcomes

Fluid responsiveness

Time Frame: intraoperative period

Cardiac output increases by more than 15% after 250 mL crystalloid injection during a fluid challenge

Study Sites (1)

Loading locations...

Similar Trials