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Effect of Post-suction Recruitment on Lung Volume in Mechanically Ventilated ICU Patients

Impact of a Recruitment Maneuver After Closed Endotracheal Suctioning on End-expiratory Lung Volume in Mechanically Ventilated ICU Patients Assessed by Electrical Impedance Tomography

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07358039
Acronym
RESPIRE
Enrollment
32
Registered
2026-01-22
Start date
2026-04-02
Completion date
2027-04-01
Last updated
2026-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mechanical Ventilation

Keywords

Endotracheal suction, Alveolar recruitment, Electrical impedance tomography, End-expiratory lung volume, Intensive care, Mechanical ventilation

Brief summary

Patients who are intubated and mechanically ventilated in the intensive care unit (ICU) require repeated endotracheal suctioning to remove airway secretions. Although this procedure is necessary, it can cause a temporary collapse of lung units (alveolar derecruitment), leading to a decrease in lung volume and impaired oxygenation. A recruitment maneuver consists of briefly applying a higher airway pressure after suctioning in order to reopen collapsed lung areas and restore lung volume. However, the clinical benefit of performing a recruitment maneuver systematically after suctioning remains uncertain. This study aims to evaluate whether performing a recruitment maneuver immediately after closed-circuit endotracheal suctioning improves lung volume compared with suctioning alone. Lung volume will be assessed using electrical impedance tomography (EIT), a non-invasive bedside imaging technique that allows real-time monitoring of lung aeration. In a randomized crossover design, each patient will undergo two suctioning procedures: one followed by a recruitment maneuver and one without, in a random order. The main outcome will be the change in end-expiratory lung volume 15 minutes after suctioning. The results may help optimize ventilatory care in mechanically ventilated ICU patients.

Detailed description

Endotracheal suctioning in mechanically ventilated ICU patients is a common procedure but is associated with alveolar derecruitment, resulting in a decrease in end-expiratory lung volume (EELV), deterioration of oxygenation, and potential lung injury. A recruitment maneuver applied immediately after suctioning may reopen collapsed alveoli and restore lung volume, provided that sufficient positive end-expiratory pressure is maintained. However, available data are limited and conflicting, especially in adult ICU patients. This prospective, randomized, open-label, single-center crossover trial will evaluate the physiological impact of a recruitment maneuver performed after closed-circuit endotracheal suctioning. Each patient will receive two interventions in random order: * Treatment A: closed-circuit endotracheal suctioning alone * Treatment B: closed-circuit endotracheal suctioning followed immediately by a recruitment maneuver (airway pressure 30 cmH₂O for 30 seconds, with unchanged PEEP) Patients will be randomized to one of two sequences (AB or BA), with a 15-minute washout period between interventions. Electrical impedance tomography (PulmoVista® V500) will be used to measure end-expiratory lung impedance, which reflects EELV. Functional residual capacity will be measured using nitrogen washout on a CARESCAPE R860 ventilator. Lung compliance and PaO₂/FiO₂ ratio will also be recorded. Measurements will be obtained before suctioning and 15 minutes after each intervention. The primary endpoint is the percentage change in EELV at 15 minutes after suctioning between the two conditions. A total of 32 mechanically ventilated ICU patients will be included.

Interventions

PROCEDURESuction + Recruitment maneuver

After suctioning, a recruitment maneuver is applied consisting of an airway pressure of 30 cmH₂O maintained for 30 seconds, without changing the positive end-expiratory pressure.

PROCEDUREClosed-circuit endotracheal suctioning

Standard closed-circuit endotracheal suctioning performed for less than 15 seconds without disconnecting the ventilator.

Sponsors

Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged ≥18 years * Covered by national health insurance * Admitted to the intensive care unit * Intubated and mechanically ventilated * Neuromuscular blockade at inclusion * Written informed consent obtained from a legally authorized representative or next of kin

Exclusion criteria

* Contraindication to electrical impedance tomography (e.g. pacemaker, implantable cardioverter-defibrillator, or implanted electrical stimulation device) * Contraindication to recruitment maneuvers (e.g. emphysema, undrained pneumothorax, hemodynamic instability) * Refractory intracranial hypertension * Acute respiratory distress syndrome requiring prone positioning * Pregnant or breastfeeding women * Patients deprived of liberty or under legal protection * Any condition judged by the investigator to interfere with study evaluation

Design outcomes

Primary

MeasureTime frameDescription
Percentage change in end-expiratory lung volume (EELV) after suctioning15 minutes after endotracheal suctioningEELV assessed by end-expiratory lung impedance measured with electrical impedance tomography (PulmoVista® V500).

Secondary

MeasureTime frameDescription
Change in lung complianceBaseline and 15 minutes after suctioningMeasured from ventilator-derived respiratory mechanics.
Change in functional residual capacity (FRC)Baseline and 15 minutes after suctioningMeasured by nitrogen washout using the CARESCAPE R860 ventilator.
Change in PaO₂/FiO₂ ratioBaseline and 15 minutes after suctioningCalculated from arterial blood gas analysis.

Countries

France

Contacts

CONTACTAsmaa JOBIC, Ph.D
asmaa.jobic@ch-toulon.fr04 83 77 20 61
PRINCIPAL_INVESTIGATORCyril PERNOD, MD

Hôpital National d'Instruction des Armées (HNIA) Sainte-Anne, Toulon

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 8, 2026