- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05001425
Association Between the Brain Excitability and Postoperative Delirium in Patients Undergoing Heart Valve Replacement Surgery With Cardiopulmonary Bypass
August 4, 2021 updated by: General Hospital of Ningxia Medical University
Association Between the Brain Excitability and Postoperative Delirium in Patients Undergoing Heart Valve Replacement Surgery With Cardiopulmonary Bypass: a Prospective Cohort Study
The purpose of this study is to explorethe brain excitability in patients undergoing heart valve replacement surgery with cardiopulmonary bypass and the correlation with postoperative delirium
Study Overview
Status
Recruiting
Detailed Description
Delirium is the most common surgical patients postoperative complications of brain dysfunction.
Delirium is a kind of consciousness attention and cognitive function changes of acute brain dysfunction, with volatility and reversibility of postoperative delirium (POD), increased hospital costs and length of hospital stay and mortality rate, and can lower the quality of life, lead to long-term postoperative cognitive dysfunction and dementia.
The incidence of postoperative cognitive dysfunction in patients undergoing cardiac valve replacement under cardiopulmonary bypass (CPB) can be as high as 44-53%.
However, since the specific mechanism of POD is still not clear, there is still a lack of effective prevention and treatment measures.
Therefore, early detection and identification are helpful for the early treatment of POD.When brain injury occurs, the levels of excitatory neurotransmitters (glutamate and aspartate) will rise in a short period of time, and the high concentration of glutamate causes excessive intracellular calcium flow, causing cellular calcium overload, and generating excitatory cytotoxic effects.
And abnormal electroencephalogram (EEG) is a kind of due to brain excitability/inhibitory amino acid imbalance caused by brain excitability increased result in abnormal discharge mode, can affect cognitive awareness and activities.
Increased brain excitability is harmful to the potential, should avoid to happen.
At present, the relationship between brain excitability and POD is still in exploring.
Therefore, it is important to clarify the correlation between brain excitability and POD in patients undergoing cardiac valve replacement under CPB for improving the pathogenesis of POD.
Study Type
Observational
Enrollment (Anticipated)
90
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Ningxia
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Yinchuan, Ningxia, China, 750004
- Recruiting
- General Hospital of Ningxia Medical University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
The patients undergoing heart valve replacement surgery with cardiopulmonary bypass
Description
Inclusion Criteria:
- ASA Ⅱ - Ⅲ;
- No cognitive impairment was assessed one day before surgery;
- Patients undergoing elective heart valve replacement under CPB and signed informed consent.
Exclusion Criteria:
- Non-CPB surgery, macrovascular surgery, heart transplantation, correction of congenital heart disease;
- Stroke, schizophrenia, depression, Parkinson's disease, epilepsy or dementia;
- Inability to communicate with language impairment or major hearing or visual impairment;
- Liver function child-pugh Grade C, severe liver dysfunction;
- Severe renal insufficiency requires preoperative renal replacement therapy;
- A past history of intraoperative knowledge.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The incidence of delirium after cardiac surgery
Time Frame: The first day after surgery
|
Postoperative evaluation delirium occurrence use the The Confusion Assessment Method(CAM) or The Confusion Assessment Method-intensive care unit(CAM-ICU).
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The first day after surgery
|
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The incidence of delirium after cardiac surgery
Time Frame: The second day after surgery
|
Postoperative evaluation delirium occurrence use the The Confusion Assessment Method(CAM) or The Confusion Assessment Method-intensive care unit(CAM-ICU).
|
The second day after surgery
|
|
The incidence of delirium after cardiac surgery
Time Frame: The third day after surgery
|
Postoperative evaluation delirium occurrence use the The Confusion Assessment Method(CAM) or The Confusion Assessment Method-intensive care unit(CAM-ICU).
|
The third day after surgery
|
|
Abnormal EEG during surgery
Time Frame: Complete EEG information from entry to exit of the operating room
|
The EEG was collected by Masimo instrument, and the EEG was recognized by the neuroelectrophysiologist, to identify whether the EEG of the patient was epileptic discharge and burst suppression during anesthesia
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Complete EEG information from entry to exit of the operating room
|
|
Plasma excitatory amino acid levels
Time Frame: Before the operation after entering the operating room (baseline)
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Venous blood 5ml was collected and centrifuged (3500r/min,10min),sera were separated and put into -80 deep temperature refrigerator for testing plasma excitatory amino acid levels.
|
Before the operation after entering the operating room (baseline)
|
|
Plasma excitatory amino acid levels
Time Frame: Immediately after surgery
|
Venous blood 5ml was collected and centrifuged (3500r/min,10min),sera were separated and put into -80 deep temperature refrigerator for testing plasma excitatory amino acid levels.
|
Immediately after surgery
|
|
Plasma excitatory amino acid levels
Time Frame: 24 hours after surgery
|
Venous blood 5ml was collected and centrifuged (3500r/min,10min),sera were separated and put into -80 deep temperature refrigerator for testing plasma excitatory amino acid levels.
|
24 hours after surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
July 1, 2020
Primary Completion (ANTICIPATED)
December 1, 2021
Study Completion (ANTICIPATED)
December 1, 2021
Study Registration Dates
First Submitted
July 27, 2021
First Submitted That Met QC Criteria
August 4, 2021
First Posted (ACTUAL)
August 12, 2021
Study Record Updates
Last Update Posted (ACTUAL)
August 12, 2021
Last Update Submitted That Met QC Criteria
August 4, 2021
Last Verified
August 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- LN 2021-1
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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