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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05209555
Other study ID # CZE-2021.57
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 10, 2022
Est. completion date December 31, 2022

Study information

Verified date April 2023
Source Catharina Ziekenhuis Eindhoven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

There is lack of attention to preoperative cognitive function and delirium in elderly who underwent surgery. The investigators are investigating different tools that can help to screen for cognitive dysfunction and delirium in the future.


Description:

Background of the study: The mean age of surgical patients is rising worldwide and this is associated with more multi-morbidity. Especially geriatric patients who undergo surgery have a higher risk to develop Postoperative Cognitive Dysfunction or a Postoperative Delirium, which leads to higher morbidity and mortality after surgery and this leads to higher healthcare costs. A delirium is an acutely disturbed state of mind characterized by restlessness, illusions, and incoherence, occurring in intoxication, fever, and other disorders and can fluctuate over time. The hypoactive delirium, the most common type of delirium, is hard to recognize compared to the active delirium that is expressed by restlessness and agitation. Postoperative cognitive dysfunction is defined as a new cognitive impairment arising after a surgical procedure. Its diagnosis requires both pre- and postoperative psychometric testing. Its manifestations are subtle and manifold, depending on the particular cognitive domains that are affected, and therefore hard to recognize too. To assess preoperative cognitive function in large groups of patients, it's needed to have a simple and quick tool to screen. In this study, the investigators use the BAMCOG, which is a tool with 3 short games played on a tablet that can provide information about cognitive functioning. When writing this new study protocol, a validation study in which the BAMCOG is validated against the MoCA is running. Beside the BAMCOG, another instrument will be investigated. The DeltaScan is an EEG delta waves measurement to identify patients with a (hypoactive) delirium. Delta waves are slow brainwaves that have been seen in sedated patients and even inpatients with an active or hypoactive delirium. A study of Kimchi et al. studied whether routine clinical EEG findings, including slowing, are correlated with delirium severity in a heterogeneous population with various causes of altered mental status and found that generalized slowing on routine clinical EEG strongly correlates with delirium and may be a valuable biomarker for delirium severity (OR 7.4, 95% CI 3.8-14.4). A lot remains unclear about the biological mechanisms in the development of a delirium after surgery, although in literature are directions that inflammatory reactions and the neuro-endocrine system play an important role. That is the reason for investigating the relation between cortisol levels in blood, saliva and sweat and the development of postoperative acute encephalopathy. Objective of the study: 1. The predictive value of the BAMCOG for developing postoperative delirium/postoperative acute encephalopathy in patients who underwent AVR surgery 2. Concurrent validation of the BAMCOG with the MoCA 3. The relation between cortisol levels in blood, saliva and sweat and the development of postoperative delirium/postoperative acute encephalopathy.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years to 120 Years
Eligibility Inclusion Criteria: - age >65 year - scheduled for AVR surgery - Able to play the BAMCOG games after instruction - (Near) native (dutch) Exclusion Criteria: - mental disorder - learning disorder - diagnosed dementia at start of study - alcohol abuses - lithium/clozapine use because of DeltaScan - sedation/RASS -4/-5 because of DeltaScan - not able to sign informed consent - implanted pacemaker, defibrillator or neurostimulator because of pilocarpine iontophoresis - history of insults - pregnant women - allergy to pilocarpine - damaged skin (forearm)

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
MoCA
MoCA test to identify Mild Cognitive Impairment
Device:
BAMCOG
Three games, compared to the MoCA to identify Mild Cognitive Impairment
Diagnostic Test:
DeltaScan
EEG to detect acute encephalopathy
Salivette
To collect saliva for cortisol analysis
Pilocarpine iontophoresis
To collect sweat for cortisol analysis

Locations

Country Name City State
Netherlands Catharina Hospital Eindhoven

Sponsors (1)

Lead Sponsor Collaborator
Catharina Ziekenhuis Eindhoven

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prognostic value of the preoperative BAMCOG to predict postoperative delirium BAMCOG and DeltaScan - preoperative 1 day, postoperative day 1, 3, 7.
Secondary Correlation BAMCOG scores and MoCA scores MoCA - preoperative 1 day, postoperative day 1, 3, 7
Secondary Prognostic value of cortisol measures (Sweat, Saliva, Serum) to predict postoperative delirium Preoperative at home and postoperative day 1
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