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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02271841
Other study ID # UCLouvain
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2014
Est. completion date December 2018

Study information

Verified date April 2021
Source Université Catholique de Louvain
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluated the practice before and after the introduction of a particular model pulsoxymeter giving, in addition, information on the state of fluid responsiveness of the patient.


Description:

This study aims to qualify the capability of general anesthesiologist to adopt Pleth Variability Index (PVI) into their practice. It also seeks to establish whether the introduction of the PVI in the clinical practice is associated with a modification of the practice. In this scope, the intent is to see the impact of introduction of PVI monitoring on anesthesiologist practices, and to do this by comparing their survey response both before and after use of PVI in their surgeries, and to see how clinical practices for GDT and outcomes may have changed. To that end, the intent is to conduct this at sites with no current experience in use of PVI parameter, so that one can closely follow the change in clinician practice as PVI is adopted.


Recruitment information / eligibility

Status Completed
Enrollment 88
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients over 18 years - ASA 1 to 3 Exclusion Criteria: - ASA 4

Study Design


Related Conditions & MeSH terms


Intervention

Device:
PVI
Pleth Variability Index

Locations

Country Name City State
Belgium Cliniques universitaires Saint-Luc Brussels

Sponsors (3)

Lead Sponsor Collaborator
Université Catholique de Louvain Universitair Ziekenhuis Brussel, Vrije Universiteit Brussel

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Other Fluid management in the elderly person in belgium Amounts and type of fluids administered. One day
Primary Practice concerning fluid management Amounts and type of fluids administered. One day
Secondary Fluid management by center Amounts and type of fluids administered. One day
Secondary Mortality after the introduction of Pleth Variability Index mortality is higher in one of the two groups? 30 days after surgery
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