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
424 participants
OBSERVATIONAL
2022-11-10
2024-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
2. The estimated operation time is more than 2 hours. 3)18≤ age ≤ 80;
4)be able to communicate normally in daily life, without serious hearing and visual impairment; 5)ASA:I-II; 6)sign informed consent and volunteer to participate in this study.
Exclusion Criteria
2. Patients with serious diseases of heart, liver, lung, kidney or other organs.
3. Having a definite diagnosis of cognitive impairment, such as Alzheimer's disease;
4. Those who use sedatives before evaluation in this study;
5. Drug addicts;
6. Alcoholics;
7. pregnant women;
8. participated in other clinical trials as a subject in the past 3 months.
18 Years
80 Years
ALL
No
Sponsors
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RenJi Hospital
OTHER
Responsible Party
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Locations
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Renji Hospital
Shanghai, , China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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SSY04070224
Identifier Type: -
Identifier Source: org_study_id
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