Effect of Lung Protective One-lung Ventilation With Fix and Variable PEEP on Oxygenation and Outcome

NCT ID: NCT03968120

Last Updated: 2024-01-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

140 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-01

Study Completion Date

2019-09-30

Brief Summary

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During One-lung ventilation, the use of lower tidal volumes (VT) is helpful to avoid over-distension, provide sufficient oxygenation, but can result in increased atelectasis.

Nevertheless, it is not known if, during one-lung ventilation with constant low VT, moderate levels of PEEP combined with lung recruitment maneuvers are superior to variable PEEP for intraoperative oxygenation and protection against PPCs.

Aim of the study is to compare a strategy using constant tidal volume with recruitment maneuvers versus variable PEEP with recruitment maneuvers during thoracic surgery in adults.

The investigators hypothesize that in adult, non-obese patients undergoing thoracic surgery under standardized OLV with variable PEEP and recruitment maneuvers as compared to constant PEEP without recruitment maneuvers prevent PPCs.

Patients will be randomly assigned to one of two groups:

FIX PEEP VOLUME GROUP (Groupfix): mechanical ventilation with constant (6 ml/kgIBW) tidal volume and PEEP of 5 cmH2O with recruitment maneuvers

VARIABLE PEEP GROUP (Groupvar): mechanical ventilation with constant (6 ml/kgIBW) tidal volume with variable PEEP with recruitment maneuvers.

Detailed Description

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Lung separation will be performed by DLT technique. Mechanical ventilation will be applied in volume-controlled mode. During two-lung ventilation, VT will be set at 8 mL/kg predicted body weight. During one-lung ventilation, in GroupFix VT will be decreased to 6 mL/kg PBW with 5 cmH2O PEEP.

In GroupVar VT mechanical ventilation with constant (6 ml/kgIBW) tidal volume with variable PEEP with recruitment maneuvers.

Conditions

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Hypoxemia Pulmonary Sepsis ARDS, Human Pneumonia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

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Group Fix:One-lung ventilation with constant PEEP

Controll group: lung protective one-lung ventilation with fix positive end-expiratory pressure (PEEP)

Group Type NO_INTERVENTION

No interventions assigned to this group

Group Variable:One-lung ventilation with variable PEEP

Variable group: lung protective one-lung ventilation with variable positive end-expiratory pressure (PEEP)

Group Type ACTIVE_COMPARATOR

Change of ventilatory settings

Intervention Type OTHER

Change of Positive End-Exspiratory Pressure during one-lung ventilation

Interventions

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Change of ventilatory settings

Change of Positive End-Exspiratory Pressure during one-lung ventilation

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient scheduled for open thoracic or video-assisted thoracoscopic surgery under general anesthesia requiring OLV (no emergency surgery)
* BMI \< 35 kg/m2
* Age ≥ 18 years
* Expected duration of surgery \> 60 min
* Expected duration of anesthesia \> 90 min

Exclusion Criteria

* COPD GOLD 3+4, lung fibrosis, documented bullae, severe emphysema, pneumothorax
* uncontrolled asthma
* NYHA 3+4, CCS 3+4
* previous thoracic surgery
* ARDS (Berlin definition)
* documented pulmonary arterial hypertension \> 40 mmHg syst
* documented or suspected neuromuscular disease (thymoma, myasthenia)
* planned mechanical ventilation after surgery
* bilateral procedures
* lung separation with other method than DLT (eg diff. airway, trachestomy)
* surgery in prone position
* persistent hemodynamic instability, intractable shock
* intracranial injury or tumor
* enrollment in other interventional study or refusal of informed consent
* pregnancy (excluded by anamnesis and/or laboratory analysis)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Debrecen

OTHER

Sponsor Role lead

Responsible Party

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Tamas Vegh, MD

Head, Division General, Vascular and Thoracic Anaesthesia

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Debrecen, Department of Anaesthesiology and Intensive Care

Debrecen, , Hungary

Site Status

Countries

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Hungary

Other Identifiers

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DE RKEB/IKEB 4918-2017

Identifier Type: -

Identifier Source: org_study_id

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