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Not yet recruiting NCT07415603

PPV vs PVI in the Supine and Prone Position

Observational Surgeries Undergoing General Anesthesia

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: Observation.
Who it may be relevant to
Registry conditions: Surgeries Undergoing General Anesthesia. Basic parameters: No limits · 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
Center list to be confirmed — check the primary protocol.
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

Variability and Correlation of the Pulse Pressure Variability (PPV) and the Plethysmography Variability Index (PVI) in the Supine and Prone Position

Overview

This is a prospective study that will record the Pulse Pressure Variability (PPV) from the arterial line and Plethysmography Variability Index (PVI) from the pulse oximeter while the patient is in the supine position and then again in the prone position. There will be no change in anesthetic care based on the study protocol. The primary objective of this study is to evaluate the changes in PVI and PPV when changing from the supine and prone position in pediatric-aged patients.

Interventions

  • Other Observation
    No intervention

Primary outcome measures

  • PPV Supine [Time frame: Once a minute for 5 minutes]
  • PVI Supine [Time frame: Once a minute for 5 minutes]
  • PPV Prone [Time frame: Once a minute for 5 minutes]
  • PVI Prone [Time frame: Once a minute for 5 minutes]

Eligibility criteria

Inclusion criteria

  • Consenting ASA 1-4 patients
  • Undergoing a surgical procedure with general anesthesia that requires placement of an arterial cannula and prone positioning

Exclusion criteria

  • Patients in whom an arterial cannula is not indicated or cannot be placed
  • Patients undergoing a surgical procedure that does not require prone positioning

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

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07415603 · STUDY00005745

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗