- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05172362
Short-Term and Long-Term Cognitive Outcomes in Adults After Cardiac Surgery
Short-Term and Long-Term Cognitive Outcomes in Adults After Cardiac Surgery: Domain-Specific Cognitive Changes, EEG and Neurovascular Unit Markers
Study Overview
Status
Detailed Description
Coronary artery bypass grafting (CABG) is one of the most effective ways to surgically correct coronary atherosclerosis. However, the postoperative cognitive decline often develops in patients who undergo CABG. According to various studies, the frequency of postoperative cognitive dysfunction (POCD) after cardiac surgery is 50-80% at the time of hospital discharge and remains present in 20-50% of patients in long-term period after surgery. The presence of POCD is associated with a decrease in surgery effectiveness and impairments in daily functioning, and is a reliable marker of unfavourable long-term prognosis (e.g., dementia and death). This prospective randomized study will be included the adult patients with stable coronary artery disease aged 45-75 years who admitted for planned CABG at the Federal State Budgetary Scientific Institution of Research Institute of Complex Issues of Cardiovascular Diseases. The study complies with the Good Clinical Practice standards and the principles of the Declaration of Helsinki. The study protocol was approved by the institutional Ethics Committee (01/2011-2520). Prior to inclusion in the study, all participants will be provided written informed consent and underwent basic cognitive screening using the Mini-Mental State Examination (MMSE) scale. The exclusion criteria are as follows: life-threatening rhythm disturbances, chronic heart failure (NYHA functional class III and higher), chronic obstructive pulmonary disease, malignant pathology, drug addiction, stroke, and other brain injuries. All the patients will be underwent general medical, neurological, instrumental examinations and extended neuropsychological assessment using the software Status PF as well as electroencephalographical examination 3-5 days before CABG, at 7-10 days after surgery and 5-7 years after CABG. POCD is determined by a 20% decrease in the cognitive indicator compared to that at baseline on 20% of the tests included in the Status PF battery. The serum concentrations of markers of the neurovascular unit (S100b, NSE, and BDNF) will be measured 3-5 days before CABG, within the first 24 h after surgery, and at 7-10 days after CABG.
In summary, the long-term neurophysiological effects following cardiac surgery are poorly understood. Moreover, little is known about the structure of cognitive impairment during the long-term postoperative period and the corresponding functional activity of the brain. The detection of minimal or subclinical signs of brain dysfunction following CABG is still under debate. Prior studies have shown the relationship between EEG abnormalities and cognitive impairment. However, little is known about EEG changes and concentrations of markers of the neurovascular unit in patients after on-pump CABG. To facilitate and improve the diagnostic accuracy, detailed neuropsychological examination using the multichannel digital EEG, serum concentrations of markers of the neurovascular unit and psychometric tests may be used to detect the long-term brain changes associated with postoperative cognitive impairment. Therefore, the study aims to evaluate the neurophysiological outcomes of patients 5-7 years after CABG.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Olga A Trubnikova, MD, PhD
- Phone Number: +73842345384
- Email: olgalet17@mail.ru
Study Locations
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Kemerovo, Russian Federation, 650002
- Recruiting
- Federal State Budgetary Scientific Institution of Research Institute of Complex Issues of Cardiovascular Diseases
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Contact:
- Olga L Barbarash, MD, PhD
- Email: olb61@mail.ru
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Planned coronary surgery
- Written informed consent
Exclusion Criteria:
- Depression (BDI-II score more than 8)
- Dementia (MMSE score less than 24; FAB score less than 11; MoCA score less than 20)
- Life-threatening rhythm disturbances
- Chronic heart failure (NYHA functional class III and higher)
- Chronic obstructive pulmonary disease
- Malignant pathology
- Drug addiction
- Stroke
- Brain injuries
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Postoperative cognitive dysfunction
Time Frame: up to 5-7 years after surgery
|
Postoperative cognitive dysfunction (POCD) is a decline in cognitive functions following surgery and anesthesia, characterized by impairment of attention, concentration, and memory that may have long-term implications. The cognitive status assessment includes extended neuropsychological testing (the assessment of psychomotor and executive function, attention, and short-term memory from the neuropsychological test battery of the psychophysiological complex software "Status PF" (Rospatent № 2001610233). |
up to 5-7 years after surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Basic cognitive status as measured by the Mini-Mental State Examination (MMSE) scale
Time Frame: up to 5-7 years after surgery
|
The Mini-Mental State Examination (MMSE) is a 30-point questionnaire that is used to measure cognitive status.The possible score in the MMSE test ranged between 0 (minimum) and 30 (maximum).The MMSE tests in this study were given in validated Russian-language versions.
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up to 5-7 years after surgery
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Basic cognitive status as measured by the Frontal Assessment Battery (FAB)
Time Frame: up to 5-7 years after surgery
|
Frontal Assessment Battery (FAB) is a test for estimation of frontal type cognitive disorders.The possible score in the FAB test ranged between 0 (minimum) and 18 (maximum).
The FAB tests in this study were given in validated Russian-language versions.
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up to 5-7 years after surgery
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Basic cognitive status as measured by the Montreal Cognitive Assessment (MoCA)
Time Frame: up to 5-7 years after surgery
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Montreal Cognitive Assessment (MoCA) is a 30-point test used for screening assessment of cognitive impairment.
MoCA scores range between 0 and 30, a score of 26 or over is considered to be normal.The MoCA tests in this study were given in validated Russian-language versions.
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up to 5-7 years after surgery
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Collaborators and Investigators
Collaborators
Investigators
- Study Director: Olga L Barbarash, MD, PhD, Research Institute for Complex Problems of Cardiovascular Diseases, Russia
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Mental Disorders
- Pathologic Processes
- Myocardial Ischemia
- Heart Diseases
- Cardiovascular Diseases
- Vascular Diseases
- Arteriosclerosis
- Arterial Occlusive Diseases
- Postoperative Complications
- Neurocognitive Disorders
- Coronary Disease
- Cognition Disorders
- Coronary Artery Disease
- Cognitive Dysfunction
- Postoperative Cognitive Complications
Other Study ID Numbers
- 01/2011-2520
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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