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Completed

NCT Number: NCT04475068

Postural Recruitment Maneuver in Patients With Acute Respiratory Distress Syndrome Due to COVID-19 Infection

The purpose of this study is to evaluate if a postural recruitment maneuver (PRM) improves the aeration and distribution of lung ventilation in patients with Acute Respiratory Distress Syndrome (ARDS) caused by COVID-19 infection; without the need to reach high airway pressures as in the standard lung recruitment maneuver and / or place the patient in prone position. This strategy could be particularly useful in the context of a major health emergency in centers with limited resources.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital Rebagliati

Jesús María, Lima, Lima 11, Peru

About this study

The PRM is based on the known effect of gravity on transpulmonary pressure (PL). Two principles explain its mechanism of action: 1) the first indicates that atelectasis and poorly ventilated areas of the lung can improve their aeration by putting the lung in the highest position. Opposite lateral decubitus causes that upper lung to have a higher PL and allow a recruiting effect at moderate airway pressures. 2) The second principle is based on Laplace's Law and postulates that once the upper lung is recruited, it remains without lung collapse if a sufficient level of positive end-expiratory pressure (PEEP) is applied. Based on these two precepts, PRM consists of sequentially moving the patient from the supine to the left lateral decubitus to recover the aeration of the right lung. After that, the patient is placed in the right lateral position to recruit the left lung; keeping the right lung without collapse by continuous use of PEEP. Finally, the patient returns to the supine position looking for an improvement in the distribution of ventilation and global pulmonary aeration, with a subsequent improvement in gas exchange and pulmonary mechanics.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients > 18 years of age
  • Patients with moderate-to-severe ARDS as per the Berlin definition
  • Infection due to COVID-19
  • Body mass index (BMI) ≤ 35 kg /m^2.

Exclusion criteria

  • Contraindication for EIT monitoring
  • Unstable spine or pelvic fractures
  • Pacemaker, automatic implantable cardioverter defibrillator
  • Skin lesions between the 4th and 5th ribs where the EIT belt is worn
  • Pregnancy
  • Major hemodynamic instability::
  • Mean arterial pressure lower than 60 mm Hg despite adequate fluid resuscitation and use of vasopressors.
  • FC> 120 or <60 per minute
  • Presence of uncontrolled arrhythmias.
  • More than 1 week of mechanical ventilation
  • Failure of more than 2 extrapulmonary organs.

Treatment and study plan

Lateral Position (left and right lateral decubitus)

Procedure

Prior to initiating the protocol, patients will be sedated deeply with sedatives and opioids and paralyzed. Patients will be evaluated in 5 positions sequentially: 1) Supine 2) Left lateral 3) Supine 4) Right lateral 5) Supine. The side with the least ventilation evaluated by EIT will define which side will start the sequence. Each step will last 30 minutes. Aeration measured by Electric Impedance Tomography (EIT) and lung ultrasound, distribution of the lung ventilation and perfusion measured by EIT, ventilator and hemodynamic parameters, esophageal pressure, and blood gas analysis will be recorded at the end of each step. Continuous monitoring of blood pressure, heart rate and saturation of arterial blood (SpO2) will be carried out during all steps of the protocol to assess the tolerance to the procedure.

Primary outcomes

  1. Effects of a postural recruitment maneuver in lung aeration

    Time frame: Through study completion (up to 24 hours)

    Lung aeration measured by ultrasound reaeration score, ranges from 0 (all regions are well aerated) to 36 (all regions are consolidated).

  2. Effects of a postural recruitment maneuver in distribution of ventilation

    Time frame: Through study completion (up to 24 hours)

    Distribution of ventilation measured by EIT (distribution and changes in the impedance in AU, arbitray units)

  3. Effects of a postural recruitment maneuver in gas exchange

    Time frame: Through study completion (up to 24 hours)

    Gas exchange measured by blood gas analysis (PaO2, PaCO2, in mmHg) and capnography (end-tidal CO2, in mmHg)

  4. Effects of a postural recruitment maneuver in respiratory mechanics

    Time frame: Through study completion (up to 24 hours)

    Respiratory mechanics measured by esophageal balloon (esophageal pressure, transpulmonary pressure, in cmH2O)

  5. Effects of a postural recruitment maneuver in hemodynamic

    Time frame: Through study completion (up to 24 hours)

    Hemodynamic data measured by invasive arterial monitoring (mean arterial pressure, in mmHg)

Secondary outcomes

  1. Feasibility of a postural recruitment maneuver

    Time frame: Through study completion (up to 24 hours)

    Oxigenatory tolerance evaluated with pulse oximeter (arterial oxygen saturation, in percentage)

Sponsors and collaborators

Lead sponsor

Hospital Nacional Edgardo Rebagliati Martins

Other

Collaborators

  • Universidad de Piura

Registry information

Official study title

Feasibility and Physiological Effects of a Postural Recruitment Maneuver in Patients With Acute Respiratory Distress Syndrome Due to COVID-19 Infection

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Jul 17, 2020
Registry last updated
Aug 25, 2021

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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