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Effect of Ventilation Mode in the Pupillary Light Reflex: A Crossover Study

Effect of Ventilation Mode in the Pupillary Light Reflex: A Crossover Study

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07082569
Acronym
EYE-BREATH
Enrollment
36
Registered
2025-07-24
Start date
2025-07-15
Completion date
2026-09-30
Last updated
2025-07-24

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

Conditions

Critical Illness, Mechanical Ventilation

Keywords

Critical illness, Mechanical ventilation, Pupillary light reflex, Automated pupillometry, Neurological Pupil Index

Brief summary

The goal of this clinical trial is to explore whether different modes of mechanical ventilation affect pupillary constriction velocities in critically ill patients without brain injury. The study aims to determine whether the type of mechanical ventilation (volume control, pressure control, or pressure-regulated volume control) influences the maximum and mean constriction velocity measured by automated pupillometry. The trial also investigates whether changes in pupil dynamics reflect subtle alterations in brainstem-autonomic interaction induced by ventilation mode. The comparison involves volume control, pressure control, and pressure-regulated volume control in a randomized crossover design to assess whether ventilation mode has a measurable effect on pupil response. Eligible participants will be intubated ICU patients receiving assist control ventilation who are not yet ready for spontaneous breathing trials. Serial pupillometry measurements will be conducted while participants are ventilated with each mode for at least 15 minutes. Sedation and lighting conditions will remain consistent throughout the protocol. Participants with acute or chronic neurologic conditions or ventilator dyssynchrony will be excluded.

Detailed description

This is a prospective, randomized, crossover study designed to evaluate the effect of different modes of mechanical ventilation on pupillary constriction velocity in critically ill patients. Recent data suggest that even in the absence of direct pulmonary or neurologic injury, mechanical ventilation with positive pressure may impact brain function, possibly through vagal-brainstem-autonomic pathways. These effects may be subtle and difficult to detect with standard neurological examination but may be reflected in changes in the dynamic pupillary light reflex. The pupillary light reflex (PLR), measured using automated infrared pupillometry, provides a quantitative, non-invasive assessment of brainstem and autonomic nervous system function. IThe investigators aim to determine whether the PLR, specifically, the mean and maximum constriction velocity, differs across three commonly used ventilation modes: Volume Control (VC), Pressure Control (PC), and Pressure-Regulated Volume Control (PRVC). All included participants will be mechanically ventilated, sedated, and not yet candidates for spontaneous breathing trials. Exclusion criteria include any acute or chronic neurologic disorder or signs of ventilator dyssynchrony. Sedation regimens (e.g., propofol, remifentanil, dexmedetomidine) will be kept constant during the study, and ambient light will remain unchanged. Each participant will undergo the three ventilation modes in a randomized order, with each mode applied for a minimum of 15 minutes to ensure washout before pupillometry measurements are performed. Physiological parameters such as respiratory rate, minute ventilation, FiO₂, heart rate, and mean arterial pressure will be recorded in parallel with pupil measurements. Blood gas analysis and full pupillometry data, including pupil size, constriction and dilation velocities, latency, and the Neurological Pupil Index (NPi), will also be collected. The primary outcome is the difference in maximum pupillary constriction velocity between ventilation modes. Secondary outcomes include mean constriction velocity, NPi, and other pupillary metrics. Based on pilot data, a total of 36 participants are required to detect a significant difference in the primary outcome. Statistical analysis will include repeated measures ANOVA or the Friedman test, with post hoc Wilcoxon Signed-Rank testing as appropriate. The findings of this study may provide support for the use of pupillometry as a tool to assess subtle CNS effects of mechanical ventilation and could support the theory of ventilation-brainstem interactions during mechanical ventilation.

Interventions

Standard mode of mechanical ventilation delivering a preset tidal volume. Commonly used in ICU patients requiring controlled ventilation.

Pressure-targeted ventilation mode that delivers breaths at a fixed pressure. Commonly used in critically ill patients.

Hybrid ventilation mode that automatically adjusts inspiratory pressure to achieve a preset tidal volume.

Sponsors

Evangelismos Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

The outcome assessor will be masked to the ventilation mode sequence applied during each pupillometry measurement. Pupillometry data will be anonymized and coded prior to statistical analysis to prevent bias in outcome evaluation.

Intervention model description

Each participant will receive three different modes of mechanical ventilation (Volume Control, Pressure Control, Pressure-Regulated Volume Control) in a randomized order. Pupillometry measurements will be taken after each mode, with a 15-minute washout period between modes.

Eligibility

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

Inclusion criteria

* Adult patients (≥18 years old) * Receiving positive-pressure mechanical ventilation * Under light or no sedation (e.g., RASS score between -2 and 0) * Clinically assessed by the treating physician as not yet ready for weaning from mechanical ventilation * Hemodynamically stable at the time of measurement * Presence of an arterial catheter in place for blood gas analysis * Written informed consent obtained from the patient's legal representative

Exclusion criteria

* Acute or chronic neurological disease affecting brainstem function or pupillary responses * Dyssynchrony with the ventilator or need for high ventilatory support adjustments * Facial injuries, edema, or conditions precluding accurate pupillometry * Use of neuromuscular blocking agents within the prior 6 hours * Severe metabolic or acid-base imbalances that may influence autonomic regulation * Concurrent participation in another interventional study that could affect neurological or autonomic outcomes

Design outcomes

Primary

MeasureTime frameDescription
Maximum Pupillary Constriction VelocityAt 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Change in maximum pupillary constriction velocity (mm/s) in response to standardized light stimulus, as measured by the NPi-200 pupillometer, under three modes of mechanical ventilation: Volume Control (VC), Pressure Control (PC), and Pressure-Regulated Volume Control (PRVC).

Secondary

MeasureTime frameDescription
Constriction LatencyAt 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Change in latency to onset of pupil constriction (seconds), measured using the NPi-200.
Dilation VelocityAt 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Change in maximum dilation velocity (mm/s) following light stimulus, measured with the NPi-200.
Neurological Pupil Index (NPi)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Change in NPi value recorded under each ventilation mode, reflecting pupillary reactivity and brainstem function.
Minimum Pupil DiameterAt 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Change in minimum pupil diameter (mm) recorded after light stimulation.
Percent ConstrictionAt 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Percent change in pupil diameter from baseline in response to light stimulus.
Maximum Pupil DiameterAt 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Change in maximum pupil diameter (mm) measured before light stimulation under each ventilation mode.

Other

MeasureTime frameDescription
Tidal Volume (mL)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Tidal volume will be recorded to ensure ventilator setting consistency.
Respiratory Rate (breaths per minute)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Respiratory rate will be recorded to monitor respiratory drive and ventilation stability.
Diastolic Blood Pressure (mmHg)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Diastolic blood pressure will be recorded during each ventilation mode to assess cardiovascular stability.
Ambient Illumination (lux)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Ambient light intensity will be recorded to confirm consistent lighting conditions for pupillometry.
Minute ventilation (L/min)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Minute ventilation will be recorded to assess ventilatory effectiveness and ensure consistency across modes.
Mean Arterial Pressure (mmHg)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Mean arterial pressure (MAP) will be recorded to evaluate overall hemodynamic stability.
Heart Rate (beats per minute)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Heart rate will be recorded to evaluate cardiovascular stability.
Arterial Partial Pressure of Oxygen, PaO₂ (mmHg)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).PaO₂ will be measured via arterial blood gas to assess oxygenation.
Exploratory Outcome Measure - Heart Rate Variability (HRV)Time interval between 15-30 minutes after the initiation of each ventilation mode (VC, PC, PRVC)HRV derived from ECG to explore autonomic nervous system modulation across ventilation modes (optional, if data acquisition becomes feasible).
Systolic Blood Pressure (mmHg)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).Systolic blood pressure will be recorded during each ventilation mode to assess cardiovascular stability.
Arterial Partial Pressure of Carbon Dioxide, PaCO₂ (mmHg)At 30 minutes after each ventilation mode initiation (VC, PC, PRVC).PaCO₂ will be measured via arterial blood gas to assess ventilation efficiency.

Countries

Greece

Contacts

Primary ContactCharikleia S. Vrettou, MD, PhD
vrettou@hotmail.com+302132105621

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026