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Brain Monitoring During PEEP-Based Respiratory Therapy in Critically Ill Patients

16 luglio 2026 aggiornato da: min xu, Shengli Oilfield Hospital

Assessment of Brain Function Changes During PEEP-Based Respiratory Therapy in Critically Ill Patients Using Multimodal Neurophysiological Monitoring

Mechanical ventilation is commonly used in critically ill patients with acute brain injury. Positive end-expiratory pressure (PEEP) and lung recruitment maneuvers are important ventilator strategies for improving oxygenation, but they may also influence cerebral blood flow, systemic hemodynamics, carbon dioxide levels, and brain electrical activity. The effects of PEEP-related ventilator changes on cortical function in neurocritical care patients remain insufficiently understood.

This prospective observational physiological study will evaluate changes in brain electrical activity and cerebral blood flow during clinically indicated lung recruitment maneuvers and PEEP adjustments in mechanically ventilated neurocritical care patients. Multimodal monitoring will include electroencephalography (EEG), transcranial Doppler ultrasound, invasive arterial blood pressure, end-tidal carbon dioxide, and routine clinical variables.

EEG-derived measures, including delta power ratio and related frequency-domain indicators, will be used to describe cortical activity. Cerebral blood flow velocity and low-frequency neurovascular coupling measures will be explored as secondary physiological outcomes. The study will examine whether PEEP-related changes are associated with alterations in EEG activity, cerebral blood flow, and neurovascular coupling, and whether these responses differ according to clinical status.

The results may help improve understanding of brain-lung interactions during mechanical ventilation and inform future studies on individualized ventilation strategies in neurocritical care.

Panoramica dello studio

Descrizione dettagliata

Acute brain injury is frequently accompanied by respiratory dysfunction requiring mechanical ventilation because of impaired consciousness, respiratory insufficiency, or the need for airway protection. Positive end-expiratory pressure (PEEP) and lung recruitment maneuvers (RM) are commonly applied to improve oxygenation and prevent alveolar collapse. Although these interventions are essential components of lung-protective ventilation, increases in intrathoracic pressure may influence venous return, systemic hemodynamics, cerebral perfusion, carbon dioxide homeostasis, and cerebral blood flow. Such physiological alterations may subsequently affect cortical activity and neurovascular coupling, particularly in patients with impaired cerebrovascular regulation. However, the cerebral effects of ventilator interventions remain incompletely understood in neurocritical care populations.

This prospective, single-center study is designed to investigate brain-lung interactions during mechanical ventilation in patients admitted to a neurocritical care unit. The study focuses on the dynamic relationships among ventilator settings, cerebral electrophysiological activity, cerebral hemodynamics, and systemic physiological responses during clinically indicated recruitment maneuvers and PEEP adjustments.

During routine respiratory management, participants will undergo predefined ventilator interventions consisting of recruitment maneuvers and PEEP modifications according to the study protocol. Physiological signals will be continuously recorded throughout baseline, intervention, and recovery periods. This design allows assessment of cerebral responses to controlled changes in intrathoracic pressure and respiratory support while minimizing interference with standard clinical care.

Multimodal physiological monitoring will be performed simultaneously throughout the study period. Monitoring modalities include scalp electroencephalography (EEG), transcranial Doppler ultrasonography (TCD), invasive arterial blood pressure monitoring, end-tidal carbon dioxide monitoring, pulse oximetry, and routine intensive care monitoring. Physiological signals from multiple monitoring devices will be synchronized and recorded using a dedicated multimodal data acquisition platform. High-resolution recordings of cerebral electrophysiological activity, cerebral blood flow velocity, arterial blood pressure, respiratory parameters, and end-tidal carbon dioxide will allow assessment of rapid physiological responses occurring during ventilator interventions. Continuous acquisition of synchronized physiological signals will permit integrated evaluation of respiratory, cardiovascular, and cerebral responses.

EEG recordings will be analyzed using quantitative electrophysiological methods to characterize cortical activity. Spectral analysis will be performed to assess changes across conventional frequency bands, including relative delta activity and other power-based indices reflecting alterations in cortical functional state. Cerebral blood flow dynamics will be evaluated using TCD-derived cerebral blood flow velocity measurements. Simultaneous recordings of arterial blood pressure and end-tidal carbon dioxide will provide complementary information regarding cerebral perfusion and respiratory physiology.

A central component of the study is the investigation of neurovascular coupling during mechanical ventilation. Integrated analysis of EEG activity and cerebral blood flow oscillations will be performed to characterize physiological coupling between neuronal activity and cerebral circulation. Relationships among cerebral electrophysiological activity, cerebral blood flow velocity, systemic hemodynamics, respiratory variables, and ventilator settings will be explored to better understand mechanisms underlying brain-lung interactions. These analyses will provide insight into how ventilator-induced physiological changes may influence cerebral function and cerebrovascular regulation in critically ill patients.

By providing simultaneous assessment of respiratory, hemodynamic, and neurophysiological responses during ventilator interventions, this study aims to improve understanding of the physiological mechanisms linking mechanical ventilation and brain function. The findings may contribute to the development of individualized ventilatory strategies that optimize respiratory support while preserving cerebral physiological stability in patients with acute brain injury.

Tipo di studio

Interventistico

Iscrizione (Stimato)

50

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Shandong
      • Dongying, Shandong, Cina, 257034
        • Reclutamento
        • Shengli Oilfield Central Hospital
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Age ≥18 years.
  • Admission to the neurocritical care unit with acute brain injury requiring intensive care management.
  • Receiving invasive mechanical ventilation.
  • Undergoing clinically indicated recruitment maneuvers and positive end-expiratory pressure (PEEP) adjustments.
  • Availability of an adequate temporal acoustic window for transcranial Doppler monitoring.
  • Written informed consent obtained from the participant or a legally authorized representative.

Exclusion Criteria:

  • Pregnancy.
  • Hemodynamic instability precluding recruitment maneuvers or PEEP adjustments.
  • Severe cardiac dysfunction judged by the treating physician to contraindicate study procedures.
  • Inability to obtain adequate transcranial Doppler signals.
  • Conditions preventing EEG monitoring, including extensive scalp injury or dressings that preclude electrode placement.
  • Withdrawal of informed consent.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Scienza basilare
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: PEEP-Based Respiratory Intervention
A standardized lung recruitment maneuver performed during mechanical ventilation to transiently increase airway pressure and reopen collapsed alveoli. Physiological responses are continuously monitored using multimodal neuromonitoring and hemodynamic monitoring systems.
Positive end-expiratory pressure (PEEP) levels are adjusted according to the study protocol during mechanical ventilation. Cerebral electrophysiological activity, cerebral blood flow, systemic hemodynamics, and respiratory parameters are continuously recorded during PEEP modifications.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in EEG Delta Power Ratio During PEEP-Based Respiratory Interventions
Lasso di tempo: During ventilator interventions (baseline, intervention, and recovery periods; approximately 30 minutes)
Change in electroencephalography (EEG)-derived delta power ratio (DPR) measured before, during, and after recruitment maneuvers and positive end-expiratory pressure (PEEP) adjustments. DPR is calculated as the proportion of delta-band power relative to total EEG power and is used as an indicator of cortical electrophysiological activity.
During ventilator interventions (baseline, intervention, and recovery periods; approximately 30 minutes)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in Cerebral Blood Flow Velocity
Lasso di tempo: During ventilator interventions (approximately 30 minutes)
Changes in cerebral blood flow velocity measured by transcranial Doppler ultrasonography during recruitment maneuvers and PEEP adjustments.
During ventilator interventions (approximately 30 minutes)
Change in Neurovascular Coupling Index
Lasso di tempo: During ventilator interventions (approximately 30 minutes)
Changes in neurovascular coupling quantified by phase-amplitude coupling analysis between low-frequency cerebral blood flow oscillations and EEG activity.
During ventilator interventions (approximately 30 minutes)
Change in Mean Arterial Pressure
Lasso di tempo: During ventilator interventions (approximately 30 minutes)
Changes in invasive mean arterial pressure during recruitment maneuvers and PEEP adjustments.
During ventilator interventions (approximately 30 minutes)

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 febbraio 2024

Completamento primario (Stimato)

1 febbraio 2027

Completamento dello studio (Stimato)

1 febbraio 2027

Date di iscrizione allo studio

Primo inviato

16 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

16 luglio 2026

Primo Inserito (Effettivo)

21 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

21 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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