Study on Biomarkers of Postoperative Delirium in Elderly Cardiac Surgery Patients
NCT ID: NCT06194474
Last Updated: 2024-01-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
24 participants
OBSERVATIONAL
2022-09-05
2024-02-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
RETROSPECTIVE
Study Groups
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Delirium Group
No interventions assigned to this group
No Delirium Group
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. American Society of Anesthesiologists (ASA) physical status of II-III and New York Heart Association grade of II-III.
3. The planned cardiac surgery.
4. Hospitalization duration not less than 5 days.
5. The anesthesia time will be no less than 2 hours.All patients had a normal ability to hear, read and cooperate with neuropsychological tests.
Exclusion Criteria
2. Patients with dementia, history of neurological or psychiatric disease, hospital with anxiety depression scale (HADS) over eight points,
3. Currently use sedatives or antidepressants, Patients with substance dependence on drugs or alcohol.
4. Patients with liver and kidney dysfunction, patients with a history of cardiac surgery.
5. Admitted to the ICU for more than two days within the month preceding the current surgery,
6. Unable to cooperate with researcher's investigations.
55 Years
80 Years
ALL
No
Sponsors
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Jining First People's Hospital
OTHER
Responsible Party
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Fuhui Yan
Study Director
Locations
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Fuhui Yan
Jining, Shandong, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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JNFPH-2023-01
Identifier Type: -
Identifier Source: org_study_id
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