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Not yet recruiting NCT06733389

Peripheral Venous Pressure Variation, Pulse Pressure Variation and Pleth Variability Index for Fluid Responsiveness

Observational Pulse Pressure Variation Stroke Volume Variation Pleth Variability Index

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: peripheral waveform collection.
Who it may be relevant to
Registry conditions: Pulse Pressure Variation, Stroke Volume Variation, Pleth Variability Index. Basic parameters: 19 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Interventions

  • Other peripheral waveform collection
    The peripheral venous pressure is collected by connecting a pressure transducer that is currently in use to the central venous line. In addition, pulse pressure variation and stroke volume variation that can be obtained from the arterial catheter. In addition, the pleth variability index is collected through the oxygen saturation monitoring. This extracts the medical records and bio-signal information of the subjects registered through the previously approved 'Establishment of a Bio-signal and C

Primary outcome measures

  • Fluid responsiveness [Time frame: intraoperative period]

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

South Korea · 1 center
  • Seoul National University Bundang Hospital — Seongnam-si

Identifiers

NCT: NCT06733389 · B-2412-941-301

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗