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Alteration of Blood-Brain-Barrier Permeability at Loss of Consciousness in Delirious Patients Recorded With Direct-Current Electroencephalography (ACDC)

Alteration of Blood-Brain-Barrier Permeability at Loss of Consciousness in Delirious Patients Recorded With Direct-Current Electroencephalography (ACDC)

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04320082
Enrollment
24
Registered
2020-03-24
Start date
2020-08-10
Completion date
2021-11-11
Last updated
2025-05-07

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

Conditions

Delirium

Brief summary

With this trial we aim to characterize the intraoperative signatures of the Direct-Current-Electroencephalogram (DC-EEG) of elderly patients developing a PostOperative Delirium (POD) compared to patients who do not develop a POD. We hereby intend to gain a better understanding of the electrical potential at the blood-brain-barrier (measured with DC-EEG) during general anaesthesia. Second, we want to study the effect of age on the DC-EEG by comparing a younger (18-30y) to an elderly cohort (\>70). Third, we aim to couple the DC-EEG signatures to blood sample analysis in order to understand the relationship between metabolic, inflammatory and vascular reaction with the intraoperative DC-EEG.

Detailed description

In order to study the intraoperative DC-EEG signatures of elderly patients coupled with lab data to evaluate the role of the age-dependent blood-brain barrier (BBB) dysfunction in general anesthesia and its meaning in POD pathophysiology following protocol will be followed: 1. On the day of the surgery the 21 DC-EEG sintered Ag/AgCl (silver chloride) electrodes will be placed before the start of anesthesia following the 10-20-system. 2. The first blood sample will be collected via the routinely placed intravenous catheter. 3. During the induction of anesthesia special care will be given to the exact time of loss of consciousness (LOC), defined with the suppression of the lid closure reflex. 4. Markers will be set at important time points of the anesthetic care (Baseline, start of analgesia/anesthesia, LOC, intubation, beginning of surgical procedure, end of anesthesia, regain of consciousness, extubation, admission recovery room). 5. Shortly after consciousness has vanished (5-10 minutes), a second blood sample will be drawn. 6. The DC-EEG recording will last until one hour after arrival at the recovery room, during which NuDesc score will be assessed every 15 minutes. 7. A third blood sample is to be collected in the recovery room. In the five days following surgery patients will be visited in the morning and in the evening to screen delirious symptoms with the help of standardized scores (NuDesc, DSM V, DDS). If patients are staying on the intensive care unit the CAM-ICU will be used. Blood sample analysis will include blood cells count, electrolytes, inflammatory markers, cholesterols, proteins, structural BBB markers and markers of neuronal damage.

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged \>70 years OR between 18 and 30 * Planned operation time \>1 hour * Expected hospital treatment period of 5 days, * Anesthesia induction, anesthesia maintenance with either Propofol or an inhalative anesthetic agent as Sevoflurane or Desflurane, * The ability to give informed consent

Exclusion criteria

* Age under 18 or between 31 and 69 * Patients with a history of neurological or psychiatric disorders * Planned neurosurgery * Current medication of tranquilizers / antidepressants * Isolation of patients with multi-resistant Bacteria * Inability of the patients to speak and/or read German * Intraoperative use of ketamine, N²O, Etomidate or Dexmedetomidine * Participation in a prospective interventional trial

Design outcomes

Primary

MeasureTime frameDescription
1. DC-Shift (µV/sec) in the perioperative DC-EEG.From the beginning of general anaesthesia to one hour after regain of consciousnessFull-brain DC-EEG with 21 electrodes placed preoperatively following the 10/20-System and recording until one hour after regain of consciousness.

Secondary

MeasureTime frameDescription
Burst suppression durationDuring anesthesia procedureFull-brain EEG recording with surface electrodes, raw EEG analysis
Incidence of Postoperative DeliriumPatients will be follow until hospital discharge, or maximal until postoperative day 5Postoperative Delirium is defined according to Diagnostic and Statistical Manual of Mental Disorders (DSM-V) and/or as ≥ 2 cumulative points in the nursing Delirium Screening Scale (Nu-DESC) and/or a positive Confusion Assessment Method (CAM) and/or Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) score and/or patient chart review that shows descriptions of Delirium.
Additional perioperative DC-EEG signatures: morphology, polarity (positive/negative), amplitude (µV)From the beginning of general anaesthesia to one hour after regain of consciousnessFull-brain DC-EEG with 21 electrodes placed preoperatively following the 10/20-System and recording until one hour after regain of Consciousness.
DC-EEG signatures in young (18-30) vs. elderly (>70) patientsFrom the beginning of general anaesthesia to one hour after regain of consciousnessFull-brain DC-EEG with 21 electrodes placed preoperatively following the 10/20-System and recording until one hour after regain of consciousness
Peri-operative, full-brain overall EEG band powerUp to the end of stay in the recovery roomFull-brain EEG recording with surface Ag/AgCl electrodes Spectral analysis by Matlab Code/Lab Chart
Duration of DeliriumParticipants will be followed for the duration of hospital stay, or maximal until postoperative day 5Diagnostic and Statistical Manual of Mental Disorders (DSM-V); Nursing Delirium Screening Scale (Nu-DESC), Confusion Assessment Method for the Intensive Care Unit (CAM-ICU), Confusion Assessment Method (CAM), Chart Review
Intensive care unit length of stayParticipants will be followed for the duration of intensive care unit stay, an expected average of 5 daysThe stay is measured in days.
Hospital length of stayParticipants will be followed for the duration of hospital stay, an expected average of 7 daysThe stay is measured in days.
Analysis of pre-, intra- and postoperative blood parameters: From shortly before the beginning of general anaesthesia to maximum one hour after arrival in the recovery roomBlood samples will be drawn before the start of general anesthesia, shortly after loss of consciousness and in the recovery room.

Countries

Germany

Outcome results

None listed

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