PPV vs PVI in the Supine and Prone Position
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 →
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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