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Very Low Tidal Volume vs Conventional Ventilatory Strategy for One-lung Ventilation in Thoracic Anesthesia

Primary Purpose

Acute Respiratory Distress Syndrome

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Protective one lung ventilation
Sponsored by
Azienda Ospedaliera S. Maria della Misericordia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Respiratory Distress Syndrome focused on measuring One lung ventilation, PEEP, thoracic surgery, lobectomy and pneumonectomy, ARDS

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients ≥ 18 years
  • ASA IV
  • Elective thoracotomies or thoracoscopic lung resection surgery (lobectomy, bilobectomy, pneumonectomy)

Exclusion Criteria:

  • Emergency surgery
  • Wedge resection or atypical resection
  • Non-resective lung surgery requiring OLV
  • Patients < 18 years
  • BMI < 20 and BMI > 29
  • Heart disease with ejection fraction <50% and/or severe valvulopathy
  • Pulmonary hypertension
  • Renal failure requiring dialytic treatment
  • Drug addiction
  • Mental retardation, depression and psychiatric disease
  • Motor or sensory deficit
  • Pregnancy

Sites / Locations

  • ASST Papa Giovanni XXIII
  • IRCCS Policlinico Sant'Orsola-Malpighi
  • Ospedale Centrale
  • Azienda Ospedaliera Brotzu - Ospedale Oncologico Businco
  • IRCCS Ospedale Policlinico San Martino
  • Fondazione IRCCS Istituto Nazionale Tumori
  • IRCCS Ospedale San Raffaele
  • Azienda Ospedaliera-Universitaria
  • Istituto Nazionale Tumori Fondazione Pascale
  • Azienda Ospedaliero-Universitaria
  • IRCCS Centro di Riferimento Oncologico della Basilicata
  • Istituto Nazionale Tumori Regina Elena
  • Azienda Ospedaliera Universitaria Senese
  • Ospedale di Cattinara
  • Department of Anesthesia and Intensive Care Unit
  • Ospedale di Circolo e Fondazione Macchi

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Protective

Conventional

Arm Description

Two-lung ventilation (TLV): tidal volume = 8 mL / kg PBW, peak airway pressure ≤ 25 cm H2O, I: E = 1:2; after lung re-expansion to the closure of the chest will set a PEEP of 5 cmH2O OLV (OLV): 4 mL / kg PBW, peak airway pressure ≤ 35 cmH2O, respiratory rate <30, I:E = 1:2 / 1:3. During OLV in case of desaturation (before increasing the FiO2) and every 60 minutes alveolar recruitment maneuvers followed by the setting of PEEP to 5 cmH2O

Two-lung ventilation (TLV): tidal volume = 8 mL / kg PBW, peak airway pressure ≤ 25 cmH2O; I: E = 1:2; after lung re-expansion to the closure of the chest PEEP set to 5 cmH2O OLV (OLV): 6 mL / kg PBW, peak airway pressure ≤ 35 cmH2O; I: E = 1:2.

Outcomes

Primary Outcome Measures

Acute Respiratory Distress Syndrome (ARDS) incidence
incidence of ARDS (%)

Secondary Outcome Measures

Postoperative pulmonary complications (PPCs)
Incidence of PPCs (%)
In-hospital mortality
To determine mortality (%)
Postoperative complications
To determine how many patients (%) would have any postoperative complications
Unplanned Intensive Care Unit (ICU) admission
To determine how many patients would require an ICU admission (%)
Intensive Care Unit (ICU) Length of stay
Length of stay in ICU (days)
Length of hospital stay
Duration of hospital length of stay

Full Information

First Posted
December 30, 2011
Last Updated
November 29, 2022
Sponsor
Azienda Ospedaliera S. Maria della Misericordia
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1. Study Identification

Unique Protocol Identification Number
NCT01504893
Brief Title
Very Low Tidal Volume vs Conventional Ventilatory Strategy for One-lung Ventilation in Thoracic Anesthesia
Official Title
Multicenter Randomized Trial on Protective Ventilation Versus Conventional Ventilation During OLV in Patients Undergoing Thoracic Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
September 2013 (Actual)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
September 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliera S. Maria della Misericordia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if a protective ventilatory strategy during one-lung ventilation (OLV) based on low tidal volume, PEEP and alveolar recruitment maneuver can reduce Acute Respiratory Distress Syndrome (ARDS) and Postoperative pulmonary complications (PPCs) after major pulmonary resection. Primary endpoint: Evaluation of postoperative ARDS incidence Secondary endpoint: Evaluation od PPC incidence and postoperative outcomes (other complications, unplanned Intensive Care Admission, hospital and ICU length of stay, in-hospital mortality)
Detailed Description
Pulmonary postoperative complications (PPCs) are the most frequent adverse events after thoracic surgery. Acute respiratory distress syndrome (ARDS) is the most severe among PPCs. Injurious mechanical ventilation is a recognized risk factor associated with ARDS and PPCs after major thoracic surgery. International literature reports a wide use of tidal volume around 5-6 ml/kg predicted body weight (PBW) during one lung ventilation (OLV) but variable use of PEEP and alveolar recruitment maneuver (ARM). The aim of this multicenter, randomized, single blind study is to determine if a protective ventilatory strategy during OLV based on low tidal volume, PEEP and alveolar recruitment maneuver compared to conventional strategy can reduce ARDS and PPCs after major pulmonary resection. Primary outcome is the incidence of in-hospital ARDS. Secondary outcomes are in-hospital incidence of postoperative pulmonary complications (PPCs), major cardiovascular events, unplanned Intensive Care Unit admission, in-hospital length of stay and mortality RANDOMIZATION Patients are randomly assigned to receive protective or conventional OLV according to a computer-generated randomization list (1:1 ratio) before anesthesia induction. Patients are blinded to the treatment. Anesthesiologists and surgeons are unblinded to the treatment during the surgical procedure and the postoperative outcome assessment. MEASUREMENTS Intraoperative collection of ventilatory settings, airway pressures, arterial blood gases analysis at the following time points: T1: two lung ventilation in supine position before placing the patient in lateral decubitus; T2: 30 minutes after OLV start; T3: 60 minutes after OLV start; T4: 20 minutes after lobectomy/pneumonectomy (during OLV); T5: 15 minutes after ARM in supine position and during two lung ventilation. Postoperative data collection 1, 12, 24, 36, 48 hours after surgery and at discharge. Arterial blood gas analysis will be performed 1 hour after extubation and 24 and 72 hours after surgery (or in case of respiratory insufficiency).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome
Keywords
One lung ventilation, PEEP, thoracic surgery, lobectomy and pneumonectomy, ARDS

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
984 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Protective
Arm Type
Experimental
Arm Description
Two-lung ventilation (TLV): tidal volume = 8 mL / kg PBW, peak airway pressure ≤ 25 cm H2O, I: E = 1:2; after lung re-expansion to the closure of the chest will set a PEEP of 5 cmH2O OLV (OLV): 4 mL / kg PBW, peak airway pressure ≤ 35 cmH2O, respiratory rate <30, I:E = 1:2 / 1:3. During OLV in case of desaturation (before increasing the FiO2) and every 60 minutes alveolar recruitment maneuvers followed by the setting of PEEP to 5 cmH2O
Arm Title
Conventional
Arm Type
No Intervention
Arm Description
Two-lung ventilation (TLV): tidal volume = 8 mL / kg PBW, peak airway pressure ≤ 25 cmH2O; I: E = 1:2; after lung re-expansion to the closure of the chest PEEP set to 5 cmH2O OLV (OLV): 6 mL / kg PBW, peak airway pressure ≤ 35 cmH2O; I: E = 1:2.
Intervention Type
Procedure
Intervention Name(s)
Protective one lung ventilation
Intervention Description
Low tidal volume, PEEP and alveolar recruitment maneuver
Primary Outcome Measure Information:
Title
Acute Respiratory Distress Syndrome (ARDS) incidence
Description
incidence of ARDS (%)
Time Frame
Hospital stay (7 days average expected)
Secondary Outcome Measure Information:
Title
Postoperative pulmonary complications (PPCs)
Description
Incidence of PPCs (%)
Time Frame
Hospital stay (7 days average expected)
Title
In-hospital mortality
Description
To determine mortality (%)
Time Frame
Hospital stay (7 days average aspected)
Title
Postoperative complications
Description
To determine how many patients (%) would have any postoperative complications
Time Frame
Hospital stay (7 days average expected)
Title
Unplanned Intensive Care Unit (ICU) admission
Description
To determine how many patients would require an ICU admission (%)
Time Frame
Hospital stay (7 days average aspected)
Title
Intensive Care Unit (ICU) Length of stay
Description
Length of stay in ICU (days)
Time Frame
Hospital stay (7 days average aspected)
Title
Length of hospital stay
Description
Duration of hospital length of stay
Time Frame
Hospital stay (7 days average expected)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients ≥ 18 years ASA IV Elective thoracotomies or thoracoscopic major lung resection surgery (lobectomy, bilobectomy, pneumonectomy) Exclusion Criteria: Emergency surgery Wedge resection or atypical resection Non-resective lung surgery requiring OLV Patients < 18 years BMI < 20 and BMI > 29 Heart disease with ejection fraction <50% and/or severe valvulopathy Pulmonary hypertension Renal failure requiring dialytic treatment Drug addiction Mental retardation, depression and psychiatric disease Motor or sensory deficit Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giorgio Della Rocca, MD, Prof
Organizational Affiliation
Azienda Ospedaliero-Universitaria S. Maria della Misericordia - Udine. Italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
ASST Papa Giovanni XXIII
City
Bergamo
Country
Italy
Facility Name
IRCCS Policlinico Sant'Orsola-Malpighi
City
Bologna
Country
Italy
Facility Name
Ospedale Centrale
City
Bolzano
Country
Italy
Facility Name
Azienda Ospedaliera Brotzu - Ospedale Oncologico Businco
City
Cagliari
Country
Italy
Facility Name
IRCCS Ospedale Policlinico San Martino
City
Genova
Country
Italy
Facility Name
Fondazione IRCCS Istituto Nazionale Tumori
City
Milan
Country
Italy
Facility Name
IRCCS Ospedale San Raffaele
City
Milan
Country
Italy
Facility Name
Azienda Ospedaliera-Universitaria
City
Modena
Country
Italy
Facility Name
Istituto Nazionale Tumori Fondazione Pascale
City
Napoli
Country
Italy
Facility Name
Azienda Ospedaliero-Universitaria
City
Padova
Country
Italy
Facility Name
IRCCS Centro di Riferimento Oncologico della Basilicata
City
Rionero In Vulture
Country
Italy
Facility Name
Istituto Nazionale Tumori Regina Elena
City
Rome
Country
Italy
Facility Name
Azienda Ospedaliera Universitaria Senese
City
Siena
Country
Italy
Facility Name
Ospedale di Cattinara
City
Trieste
Country
Italy
Facility Name
Department of Anesthesia and Intensive Care Unit
City
Udine
ZIP/Postal Code
33100
Country
Italy
Facility Name
Ospedale di Circolo e Fondazione Macchi
City
Varese
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
20829341
Citation
Yang M, Ahn HJ, Kim K, Kim JA, Yi CA, Kim MJ, Kim HJ. Does a protective ventilation strategy reduce the risk of pulmonary complications after lung cancer surgery?: a randomized controlled trial. Chest. 2011 Mar;139(3):530-537. doi: 10.1378/chest.09-2293. Epub 2010 Sep 9.
Results Reference
background
PubMed Identifier
19317902
Citation
Licker M, Diaper J, Villiger Y, Spiliopoulos A, Licker V, Robert J, Tschopp JM. Impact of intraoperative lung-protective interventions in patients undergoing lung cancer surgery. Crit Care. 2009;13(2):R41. doi: 10.1186/cc7762. Epub 2009 Mar 24.
Results Reference
background

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Very Low Tidal Volume vs Conventional Ventilatory Strategy for One-lung Ventilation in Thoracic Anesthesia

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