Volumetric Monitoring in Major Lung Surgery

The hypothesis of this observational single-center clinical study was to explore the volumetric hemodynamic monitoring in the perioperative period in major and risky thoracic intervention. The investigators monitored the changes in the volumes of blood in the central vessels and heart chambers as well as a volume of fluid in pulmonary tissue (i. e. extravascular lung water).

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Key information

Conditions

Pneumonectomy Acute Pulmonary Edema

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Regional Hospital of Arkhangelsk

Arkhangelsk, Arkhangelskaya oblast, 163000, Russia

About this study

The goal of this observational study is to investigate into changes in volumetric hemodynamic parameters obtained with a technique of transpulmonary indicator dilution after major thoracic intervention, including pneumonectomy and lobar resections. The important parameters of hemodynamics were monitored throughout the intervention and 48 hrs postoperatively, including extravascular lung water index, global end-diastolic volume index, etc.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Informed consent
Age above 18 and below 80
Confirmed malignant bronchial neoplasm or
Destructive pulmonary infection

Exclusion criteria

Pregnant
Severe pulmonary hypertension
Pulmonary tuberculosis
Severe occlusive atherosclerosis of lower extremities

Sponsors and collaborators

Lead sponsor

Northern State Medical University

Other

Collaborators

Regional hospital of Arkhangelsk
University of Tromso

Registry information

Official study title

Pulmonary Edema Following Major Thoracic Resections: a Value of Perioperative Volumetric Monitoring

Acronym: EVLW-PNEUMO

Important dates

Study start: 2005
Primary completion: 2008
Study completion: 2011
First posted: Oct 20, 2011
Registry last updated: Sep 5, 2012

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.

Published trials that share one or more normalized conditions with this study.

Completed