Postoperative Neurocognitive DysfunctionINOCSNCT07200726
The Role of Neuroinflammation on Neurocognitive Outcome in Cardiac Surgery
An observational study of Postoperative Neurocognitive Dysfunction and Postoperative Neurocognitive Disorder, run by Ziekenhuis Oost-Limburg at 1 site in Belgium.
Trial summary
RATIONALE: Postoperative cognitive changes are common after cardiac surgery and can be categorised into three main types: postoperative delirium (POD), delayed neurocognitive recovery (DNCR) and postoperative neurocognitive disorder (PNCD). Read more about this study
- Who is it for?
- Ages 60 years and older
- Conditions the study is for
- Postoperative Neurocognitive Dysfunction, Postoperative Neurocognitive Disorder, Cardiac Surgery
- How many people
- 89 participants
- Where
- 1 siteBelgium
- Study dates
- 21 Oct 2025to 26 Oct 2026
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Since, compared to younger patients undergoing major surgery, elderly patients are more prone to develop PNCD and are at greater risk of morbidity, we will therefore include patients aged 60 years or older scheduled for cardiac surgery.
Who may be able to join
- aged 60 years or older;
- scheduled for cardiac surgery.
Who cannot join
- dementia, as diagnosed by a specialist, since this would make detection of PNCD impossible;
- urgent, not elective surgery.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Role of Neuroinflammation on Neurocognitive Outcome in Cardiac Surgery: INOCS Study
RATIONALE: Postoperative cognitive changes are common after cardiac surgery and can be categorised into three main types: postoperative delirium (POD), delayed neurocognitive recovery (DNCR) and postoperative neurocognitive disorder (PNCD). DNCR is diagnosed until postoperative day 30 and PNCD is diagnosed at least 30 days after the operation. Both conditions can be mild or major, and can affect the quality of life of these patients.
The incidence of PNCD in cardiac surgery is around 40%. Despite this high incidence, screening for PNCD is absent in current postoperative care since the diagnosis of PNCD is difficult and very time intensive. Furthermore, the underlying pathogenesis is incompletely understood.
Read more
The identification of a biomarker and/or validated short diagnostic instrument would be of paramount importance to easily identify patients at risk, or to diagnose patients with PNCD in order to identify therapeutical pathways for this disease.
OBJECTIVES: The main objective of this prospective clinical trial is to evaluate the performance of the short NPA and/or biochemical markers for the diagnosis of DNCR and PNCD in cardiac surgery patients aged 60 years or older.
STUDY DESIGN: Single-centre interventional observational study
STUDY INTERVENTIONS: Patients will undergo a neurophysiological assessment (NPA) pre-operatively and at two timepoints post-operatively, namely 6 (+/-1) days and 40 (+/- 10) days after surgery. During the stay at the intensive care unit, they will be screened daily for delirium, using the CAM-ICU and 3D-CAM.
To evaluate whether the development of DNCR or POD has an important effect on quality of recovery , the quality of recovery scale 15 (QOR-15), muscle strength (handgrip strength) and the Chalder fatigue score will be scored post-operative (postop day 1, 3 and 5). To evaluate whether PNCD has an effect on quality of live the EQ5D5L score will be measured at 40 (+/- 10) days after surgery, compared to preoperative values.
On several time points, blood samples will be drawn to measure markers of neuroinflammation. The time points will be preoperatively, at the moment of arrival on ICU, postoperative day 1, 2 and 3, if still on ICU. Two repeat blood sample will be taken at the moment of NPA performed after 6 (+/- 1) days and 40 (+/- 10) days after surgery, if the patient is willing (not obligatory).
STUDY POPULATION:
Patients aged 60 years or older who are scheduled for cardiac surgery.
Inclusion criteria:
- aged 60 years or older;
- scheduled for cardiac surgery.
Exclusion criteria:
- dementia, as diagnosed by a neurologist;
- urgent, not elective surgery.
MAIN STUDY ENDPOINTS:
Primary outcome PNCD defined as a decline of > 1 SD on > 2 tests in one or more cognitive domains or a decline of > 1 SD on total cognitive domain score.
Secondary outcomes Postoperative delirium - CAM-ICU will be evaluated twice daily (morning and evening) on every day when the patient is awake (not intubated) on the ICU. This is standard of care and is part of the routine clinical care in the hospital. Furthermore, once daily a 3D-CAM will be performed on day 1, 3 and 5.
Quality of recovery
- QOR-15, a validated measurement of quality of recovery in the short term postoperative recovery, will be evaluated pre-operatively and postoperatively day 1, 3 and 5.
- EQ5D5L, a validated measurement of quality of recovery in the long term postoperative recovery, will be evaluated preoperatively and at the moment of the third NPA measurement.
- Postoperative muscle function (upper extremity, by hand grip strength) on day 1, 3 and 5 after surgery and at the moment of the second and third NPA measurement (being day 6 (+/-1) and day 40 (+/-10) postoperatively), as compared to preoperative values.
- Chalder Fatigue questionnaire on day 1, 3 and day 5 and on the second and third NPA measurement, as compared to preoperative.
Biochemical analysis
- Blood samples will be drawn for analysis before induction of anaesthesia (preoperatively), at the end of the operation (immediately postoperatively on arrival in ICU), on day 1, 2 and 3 postoperatively (if still at the ICU) and at the time of the postoperative follow-up visits with the NPA testing (day 6 (+/-1) and day 40 (+/-10) days post-surgery).
At each time point, markers of neuroinflammation and -degeneration will be determined.
Tertiary outcomes
- Length of CPB
- Duration of mechanical ventilation
- Administered anaesthetic drugs during surgery
- Transfusion need
- Length of ICU stay (days)
- Length of in-hospital stay (days)
- Readmission to ICU or hospital within 28 days after surgery
- Cardiovascular outcome: atrial fibrillation, , thrombo-embolic events, myocardial injury, myocardial infarction, cardiac arrest, cardiac death
- Pulmonary outcome: postoperative pulmonary complications, postoperative pneumonia, postoperative respiratory failure
- Postoperative infection within 28 days after surgery
- Conditions
- Postoperative Neurocognitive Dysfunction, Postoperative Neurocognitive Disorder, Cardiac Surgery, Major Surgery Under General Anesthesia, Major Surgery in Adult Patients, Postoperative Fatigue
- Being tested
- Observational study design - no intervention
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Observational study design - no interventionOther
Observational study design - no intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
Incidence of postoperative neurocognitive disorder (PNCD) after cardiac surgery using the NPA.
The neuropsychological assessment (NPA) consists of 17 subsets which can be divided into five cognitive domains: speed and attention, memory, language, executive and visuospatial functioning. The outcomes are 21 scores, namely the scores of the 17 subsets and 4 combined scores. These are reported in T-scores after correction for age and educational level by comparison with a norm group. PNCD is defined as a decline of > 1 SD on > 2 tests in one or more cognitive domains or a decline of > 1 SD on total cognitive domain score.
Measured: The NPA will be taken preoperatively and postoperatively on day 40 (+/- 10).
Secondary outcomes (10)
Delayed neurocognitive recovery (DNCR)
Neurocognitive disorder early after surgery (< 30 days) will be assessed using the NPA (similar to the primary outcome).
Measured: Day 6 (+/- 1) following surgery.
Postoperative delirium (CAM-ICU)
To assess postoperative delirium on the ICU the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) questionnaire will be done twice daily (morning and evening) every day when the patient is in the ICU. The CAM-ICU is a structured assessment tool. Based on the patient's responses and performance, it is determined whether delirium is present or not.
Measured: Twice daily (morning and evening) day 1 - day 5 following surgery if the patient is still in the ICU.
Postoperative delirium (3D-CAM)
To assess postoperative delirium the 3 minute confusion assessment method (3D-CAM) questionnaire will be done on day 1, day 3 and day 5 postoperatively. The 3D-CAM consists of a structured interview and cognitive testing. Based on the patient's responses and performance, it is determined whether delirium is present or not.
Measured: Postoperative day 1, day 3 and day 5.
Quality of recovery (QoR-15)
Quality of Recovery Score (QoR-15 score) is a patient-reported outcome measurement which will be used to assess the early postoperative health status of the patient after surgery and anaesthesia, i.e. the quality of recovery. The score is arbitrary and ranges from 0 to 150, the higher the score the better the quality of recovery.
Measured: Preoperative, postoperative day 1, day 3 and day 5.
Postoperative muscle strength (HGS)
Postoperative muscle strength (upper extrimity) will be assessed by comparing the handgrip strength (HGS) of the dominant hand, measured on day 1, day 3, day 5, day 6 (+/- 1), and day 40 (+/- 10) following surgery as compared to the preoperative value.
Measured: Preoperative, postoperative day 1, day 3, day 5, day 6 (+/- 1), and day 40 (+/- 10).
Postoperative fatigue (CFQ)
To assess general fatigue a fatigue questionnaire, the Chalder fatigue questionnaire (CFQ), will be taken on day 1, day 3, day 4, day 6 (+/- 1) and day 40 (+/- 10) postoperatively. The questionnaire consists of 11 items that assess both physical and mental aspects of fatigue. Respondents rate each item ranging from 0 to 3, the scores are then totaled to provide a measure of overall fatigue, a higher score meaning more severe fatigue.
Measured: Preoperative, postoperative day 1, day 3, day 5, day 6 (+/- 1), and day 40 (+/- 10).
Health-related quality of life (EQ5D5L)
The EQ-5D-5L is used for measuring health-related quality of life. EQ-5D-5L provides a simple descriptive profile and a single index value for health status, both can be used to assess overall helaht. The descriptive profile consists of five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels of severity: no problems, slight problems, moderate problems, severe problems, or not able. Respondents select the level that best describes their current health status. The EQ-5D-5L also includes a visual analog scale (VAS) where respondents rate their current health status on a scale from 0 to 100, with 0 being the worst imaginable health state and 100 being the best imaginable health state.
Measured: Preoperative and postoperative day 40 (+/- 10).
Subjective sleep quality (PSQI)
To assess subjective sleep quality the Pittsburgh Sleep Quality Index (PSQI) will be used. The PSQI consists of 19 items that assess different components of sleep, including sleep latency, sleep duration, sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction due to poor sleep quality. Each item is rated on a scale from 0 to 3, with higher scores indicating worse sleep quality. The scores from all 19 items are summed to provide a total score ranging from 0 tot 21, with higher scores indicating poorer sleep quality. The questionnaire will be filled in 3 times: before surgery, day 6 (+/-1) and day 40 (+/- 10) after surgery.
Measured: Preoperative, postoperative day 6 (+/- 1), and day 40 (+/- 10).
Sleeping EEG pattern
Electroencephalographic (EEG) readings will be conducted during the first postoperative night to asses sleep architecture.
Measured: First postoperative night.
Markers of neuroinflammation and neurodegeneration
Blood samples will be drawn for analysis before induction of anaesthesia (preoperatively), at the end of surgery on arrival in ICU, on day 1, 2 and 3 postoperatively (if still in the ICU) and at the time of follow-up visits on day 6 (+/- 1) and day 40 (+/- 10) post-surgery. Markers of neuroinflammation and neurodegeneration (Phospho-Tau, NfL) will be determined.
Measured: Before induction of anaesthesia, immediately postoperative (on arrival in ICU), day 1, day 2 and day 3 postoperative (if still in ICU), day 6 (+/- 1) and day 40 (+/- 10).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Oct 2025
- Study start21 Oct 2025
- Primary completion26 Oct 2026
- Study completion26 Oct 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Postoperative Neurocognitive DysfunctionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 89 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ziekenhuis Oost-Limburg
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07200726
- Sponsor's protocol ID
- Z-2025013
- Acronym
- INOCS
- Status last verified
- Jul 2025
- First submitted
- 5 Sep 2025
- Last updated
- 6 Nov 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Role of Neuroinflammation on Neurocognitive Outcome in Cardiac Surgery: INOCS Study
- ClinicalTrials.gov ID
- NCT07200726
- Acronym / sponsor ID
- INOCS / Z-2025013
- Conditions
- Postoperative Neurocognitive Dysfunction, Postoperative Neurocognitive Disorder, Cardiac Surgery, Major Surgery Under General Anesthesia, Major Surgery in Adult Patients, Postoperative Fatigue
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 89 participants (actual)
- Lead sponsor
- Ziekenhuis Oost-LimburgUniversity, hospital or other
- Study start
- 21 Oct 2025 (actual)
- Primary completion
- 26 Oct 2026 (actual)
- Study completion
- 26 Oct 2026 (actual)
- First posted
- 1 Oct 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
RATIONALE: Postoperative cognitive changes are common after cardiac surgery and can be categorised into three main types: postoperative delirium (POD), delayed neurocognitive recovery (DNCR) and postoperative neurocognitive disorder (PNCD). DNCR is diagnosed until postoperative day 30 and PNCD is diagnosed at least 30 days after the operation. Both conditions can be mild or major, and can affect the quality of life of these patients.
The incidence of PNCD in cardiac surgery is around 40%. Despite this high incidence, screening for PNCD is absent in current postoperative care since the diagnosis of PNCD is difficult and very time intensive. Furthermore, the underlying pathogenesis is incompletely understood.
The identification of a biomarker and/or validated short diagnostic instrument would be of paramount importance to easily identify patients at risk, or to diagnose patients with PNCD in order to identify therapeutical pathways for this disease.
OBJECTIVES: The main objective of this prospective clinical trial is to evaluate the performance of the short NPA and/or biochemical markers for the diagnosis of DNCR and PNCD in cardiac surgery patients aged 60 years or older.
STUDY DESIGN: Single-centre interventional observational study
STUDY INTERVENTIONS: Patients will undergo a neurophysiological assessment (NPA) pre-operatively and at two timepoints post-operatively, namely 6 (+/-1) days and 40 (+/- 10) days after surgery. During the stay at the intensive care unit, they will be screened daily for delirium, using the CAM-ICU and 3D-CAM.
To evaluate whether the development of DNCR or POD has an important effect on quality of recovery , the quality of recovery scale 15 (QOR-15), muscle strength (handgrip strength) and the Chalder fatigue score will be scored post-operative (postop day 1, 3 and 5). To evaluate whether PNCD has an effect on quality of live the EQ5D5L score will be measured at 40 (+/- 10) days after surgery, compared to preoperative values.
On several time points, blood samples will be drawn to measure markers of neuroinflammation. The time points will be preoperatively, at the moment of arrival on ICU, postoperative day 1, 2 and 3, if still on ICU. Two repeat blood sample will be taken at the moment of NPA performed after 6 (+/- 1) days and 40 (+/- 10) days after surgery, if the patient is willing (not obligatory).
STUDY POPULATION:
Patients aged 60 years or older who are scheduled for cardiac surgery.
Inclusion criteria:
- aged 60 years or older;
- scheduled for cardiac surgery.
Exclusion criteria:
- dementia, as diagnosed by a neurologist;
- urgent, not elective surgery.
MAIN STUDY ENDPOINTS:
Primary outcome PNCD defined as a decline of > 1 SD on > 2 tests in one or more cognitive domains or a decline of > 1 SD on total cognitive domain score.
Secondary outcomes Postoperative delirium - CAM-ICU will be evaluated twice daily (morning and evening) on every day when the patient is awake (not intubated) on the ICU. This is standard of care and is part of the routine clinical care in the hospital. Furthermore, once daily a 3D-CAM will be performed on day 1, 3 and 5.
Quality of recovery
- QOR-15, a validated measurement of quality of recovery in the short term postoperative recovery, will be evaluated pre-operatively and postoperatively day 1, 3 and 5.
- EQ5D5L, a validated measurement of quality of recovery in the long term postoperative recovery, will be evaluated preoperatively and at the moment of the third NPA measurement.
- Postoperative muscle function (upper extremity, by hand grip strength) on day 1, 3 and 5 after surgery and at the moment of the second and third NPA measurement (being day 6 (+/-1) and day 40 (+/-10) postoperatively), as compared to preoperative values.
- Chalder Fatigue questionnaire on day 1, 3 and day 5 and on the second and third NPA measurement, as compared to preoperative.
Biochemical analysis
- Blood samples will be drawn for analysis before induction of anaesthesia (preoperatively), at the end of the operation (immediately postoperatively on arrival in ICU), on day 1, 2 and 3 postoperatively (if still at the ICU) and at the time of the postoperative follow-up visits with the NPA testing (day 6 (+/-1) and day 40 (+/-10) days post-surgery).
At each time point, markers of neuroinflammation and -degeneration will be determined.
Tertiary outcomes
- Length of CPB
- Duration of mechanical ventilation
- Administered anaesthetic drugs during surgery
- Transfusion need
- Length of ICU stay (days)
- Length of in-hospital stay (days)
- Readmission to ICU or hospital within 28 days after surgery
- Cardiovascular outcome: atrial fibrillation, , thrombo-embolic events, myocardial injury, myocardial infarction, cardiac arrest, cardiac death
- Pulmonary outcome: postoperative pulmonary complications, postoperative pneumonia, postoperative respiratory failure
- Postoperative infection within 28 days after surgery
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 60 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Since, compared to younger patients undergoing major surgery, elderly patients are more prone to develop PNCD and are at greater risk of morbidity, we will therefore include patients aged 60 years or older scheduled for cardiac surgery.
Key inclusion criteria (2 listed)
- aged 60 years or older;
- scheduled for cardiac surgery.
Key exclusion criteria (2 listed)
- dementia, as diagnosed by a specialist, since this would make detection of PNCD impossible;
- urgent, not elective surgery.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Observational study design - no interventionObservational study design - no intervention | Other | – |
Primary outcome
Incidence of postoperative neurocognitive disorder (PNCD) after cardiac surgery using the NPA.
Time frame: The NPA will be taken preoperatively and postoperatively on day 40 (+/- 10).
The neuropsychological assessment (NPA) consists of 17 subsets which can be divided into five cognitive domains: speed and attention, memory, language, executive and visuospatial functioning. The outcomes are 21 scores, namely the scores of the 17 subsets and 4 combined scores. These are reported in T-scores after correction for age and educational level by comparison with a norm group. PNCD is defined as a decline of > 1 SD on > 2 tests in one or more cognitive domains or a decline of > 1 SD on total cognitive domain score.
10 secondary outcomes
Delayed neurocognitive recovery (DNCR)
Time frame: Day 6 (+/- 1) following surgery.
Postoperative delirium (CAM-ICU)
Time frame: Twice daily (morning and evening) day 1 - day 5 following surgery if the patient is still in the ICU.
Postoperative delirium (3D-CAM)
Time frame: Postoperative day 1, day 3 and day 5.
Quality of recovery (QoR-15)
Time frame: Preoperative, postoperative day 1, day 3 and day 5.
Postoperative muscle strength (HGS)
Time frame: Preoperative, postoperative day 1, day 3, day 5, day 6 (+/- 1), and day 40 (+/- 10).
Postoperative fatigue (CFQ)
Time frame: Preoperative, postoperative day 1, day 3, day 5, day 6 (+/- 1), and day 40 (+/- 10).
Health-related quality of life (EQ5D5L)
Time frame: Preoperative and postoperative day 40 (+/- 10).
Subjective sleep quality (PSQI)
Time frame: Preoperative, postoperative day 6 (+/- 1), and day 40 (+/- 10).
Sleeping EEG pattern
Time frame: First postoperative night.
Markers of neuroinflammation and neurodegeneration
Time frame: Before induction of anaesthesia, immediately postoperative (on arrival in ICU), day 1, day 2 and day 3 postoperative (if still in ICU), day 6 (+/- 1) and day 40 (+/- 10).
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Nov 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Postoperative Neurocognitive Dysfunction and Postoperative Neurocognitive Disorder, run by Ziekenhuis Oost-Limburg at 1 site in Belgium.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Belgium. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Incidence of postoperative neurocognitive disorder (PNCD) after cardiac surgery using the NPA. (time frame: The NPA will be taken preoperatively and postoperatively on day 40 (+/- 10).). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Nov 2026.