Effects of Perioperative Operating Room Environment on Postoperative Delirium
NCT ID: NCT05551026
Last Updated: 2023-10-23
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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UNKNOWN
360 participants
OBSERVATIONAL
2022-08-22
2024-02-26
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* ASA I-III;
* Patients who plan to undergo elective abdominal surgery under general anesthesia;
* Volunteer to participate in this study and sign informed consent.
Exclusion Criteria
* Severe vision, hearing, language impairment or other reasons unable to communicate with visitors;
* Severe dysfunction of important organs such as heart, brain, lung, liver, kidney, etc.;
* Long-term use of sedatives, antidepressants or alcoholism;
* Patients with severe postoperative complications and admitted to intensive care unit;
* Patients who refused or failed to complete the cognitive function test.
* Patients who could not cooperate with the study for any other reason.
65 Years
90 Years
ALL
No
Sponsors
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The Second Affiliated Hospital of Chongqing Medical University
OTHER
Responsible Party
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Principal Investigators
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Jia Tang, MD
Role: STUDY_DIRECTOR
Department of Anesthesiology, The Second Affiliated Hospital, Chongqing Medical University
Locations
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Department of Anesthesiology, The Second Affiliated Hospital, Chongqing Medical University
Chongqing, Chongqing Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Factors of POD
Identifier Type: -
Identifier Source: org_study_id
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