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OpenTrials
Completed

NCT Number: NCT00816153

Pleth Variability Index and Fluid Management During Surgery

Pleth Variability Index (PVI) seems to be an ideal parameter to guide fluid management: dynamic parameter and non-invasive. PVI could guide fluid management during surgery and optimization of the plethysmographic-derived parameter could improve hemodynamics of the patients.

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Key information

Conditions

Fluid Management

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St-Luc Hospital

Brussels, 1200, Belgium

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Major abdominal surgery

Exclusion criteria

  • Refusal or inability to understand the protocol
  • Arrythmia
  • <18 years
  • Contraindication to normal mechanical ventilation

Treatment and study plan

PVI-guided fluid management

Other

Peroperative comparison of standard care with PVI-guided fluid management (optimization of the PVI value with fluid loading)

Primary outcomes

  1. Hemodynamics and derived-parameters

    Time frame: The first 48 h

Secondary outcomes

  1. All causes of morbi-mortality

Sponsors and collaborators

Lead sponsor

Université Catholique de Louvain

Other

Collaborators

  • Masimo Corporation

Registry information

Official study title

Is Pleth Variability Index Able to Guide Fluid Management During Surgery?

Important dates

Study start
2008
Primary completion
2008
Study completion
2008
First posted
Dec 31, 2008
Registry last updated
Dec 31, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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