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Prevention of Lung Edema After Thoracic Surgery

This study has been completed.

Sponsored by: University Hospital, Geneva
Information provided by: University Hospital, Geneva
ClinicalTrials.gov Identifier: NCT00498251
  Purpose

Background :

Acute lung injury (ALI) occasionally occurs after pulmonary resection and carries a bad prognosis with a high mortality rate ranging from 20 to 100%.

Objectives :

  1. to evaluate pre-, intra- and postoperative changes in hemodynamics, oxygenation indices as well as intra- and extravascular lung water using simple thermodilution technique and continuous arterial pressure analysis
  2. to test the efficacy of inhaled beta2 -adrenergic agonist versus anticholinergic agents to reduce lung edema in patients undergoing thoracic surgery and in pigs subjected to lipolysacharide-induced ALI.

Design of the research protocol:

  • Prospective controlled trial including surgical patients with high risk factors for ALI (n=60) allocated to receive inhaled drugs (randomised, double-blind, cross-over mode).
  • Main measurements:

Intra-thoracic blood volume, intra- and extra-vascular lung water, hemodynamic parameters (CO, systolic arterial pressure/flow variations, dPmax, MAP, CVP), oxygenation indices (PaO2/FIO2), ventilatory parameters, clinical outcome data, histochemical and pathological data.

Glossary CO = cardiac output; dPmax = maximal arterial pressure slope; SAP-V = systolic arterial pressure variations; Flow–V = Flow variations; MAP = mean arterial pressure; CVP = central venous pressure; PaO2=arterial oxygen pressure; FIO2= oxygen inspiratory fraction


Condition Intervention
Lung Injury, Acute
Thoracotomy
Anesthesia
Intensive Care, Surgical
Extravascular Lung Water
Drug: inhalation of salbutamol (5 mg)
Drug: ipratropium

MedlinePlus related topics:   Anesthesia    Drinking Water    Edema   

ChemIDplus related topics:   Albuterol sulfate    Albuterol    Levalbuterol hydrochloride    Levalbuterol tartrate    Ipratropium    Ipratropium bromide   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Active Control, Crossover Assignment, Efficacy Study
Official Title:   Does Inhaled Salbutamol Prevent Lung Edema After Thoracic Surgery? A Randomized Controlled Study

Further study details as provided by University Hospital, Geneva:

Primary Outcome Measures:
  • reduction in extravascular lung water [ Time Frame: within the first 24 hours after lung surgery ]

Secondary Outcome Measures:
  • changes in oxygenation indices, hemodynamics and radiological lung injury score [ Time Frame: within the first 48 hours ]

Enrollment:   30
Study Start Date:   September 2004
Study Completion Date:   June 2007

Show detailed description  Show Detailed Description

  Eligibility
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

Patients with at least 3 risk factors for postoperative lung edema

  • age > 60 yrs
  • history of chronic alcohol consumption (>60g/day)
  • prior radiation or chemotherapy
  • cardiac insufficiency (left ventricular ejection fraction < 40%, or a history of past acute heart failure)
  • coronary artery disease (history of myocardial infarct, Q wave on the ECG, positive stress test or coronary angiogram)
  • recent pneumonia (within 6 weeks of hospital admission)
  • reduced diffusion capacity for carbon monoxide (DLCO < 60% of predicted values)
  • predicted postoperative lung perfusion of < 55% of total lung perfusion

Exclusion Criteria:

  • pneumonectomy
  • intracardiac shunts
  • valvular diseases
  • aortic abdominal aneurysm
  • chronic treatment with inhaled bronchodilators
  • a history of any adverse reaction to bronchodilators
  • liver or kidney insufficiencies
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00498251

Locations
Switzerland
University Hospital of Geneva    
      Geneva, Switzerland, CH-1211

Sponsors and Collaborators
University Hospital, Geneva

Investigators
Principal Investigator:     Christoph Ellenberger, MD     University Hospital of Geneva    
  More Information


Publications indexed to this study:

Study ID Numbers:   CER03-160
First Received:   July 6, 2007
Last Updated:   July 9, 2007
ClinicalTrials.gov Identifier:   NCT00498251
Health Authority:   Switzerland: Ethikkommision

Keywords provided by University Hospital, Geneva:
lung injury, acute  
thoracic surgical procedures  
lung cancer  
salbutamol  

Study placed in the following topic categories:
Pulmonary Edema
Ipratropium
Respiratory Tract Diseases
Lung Neoplasms
Lung Diseases
Albuterol
Respiration Disorders
Respiratory Distress Syndrome, Adult
Edema
Acute respiratory distress syndrome

Additional relevant MeSH terms:
Respiratory System Agents
Neurotransmitter Agents
Cholinergic Antagonists
Molecular Mechanisms of Pharmacological Action
Adrenergic beta-Agonists
Adrenergic Agents
Physiological Effects of Drugs
Anti-Asthmatic Agents
Reproductive Control Agents
Cholinergic Agents
Pharmacologic Actions
Adrenergic Agonists
Tocolytic Agents
Autonomic Agents
Therapeutic Uses
Peripheral Nervous System Agents
Bronchodilator Agents

ClinicalTrials.gov processed this record on October 06, 2008




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