Effect of Preoperative Sarcopenia on Postoperative Delirium in Elderly Patients Undergoing Gastrointestinal Surgery
NCT ID: NCT05847296
Last Updated: 2023-05-09
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
334 participants
OBSERVATIONAL
2023-05-05
2024-02-01
Brief Summary
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• Effect of preoperative sarcopenia on postoperative delirium in elderly patients undergoing gastrointestinal surgery Participants will be evaluated preoperatively for sarcopenia and assessed for postoperative delirium, pain, etc.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Sarcopenia group
No interventions assigned to this group
Non sarcopenic group
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Patients to undergo elective abdominal surgery (gastrointestinal tumor resection) under general anesthesia, with an expected operation duration of about 2h\~4h
3. ASA Ⅰ-Ⅲ
Exclusion Criteria
2. Abnormal renal and liver function: AST or ALT≥2.5×ULN, TBIL≥1.5×ULN, Serum creatinine concentration (SCC)≥1.5×ULN
3. People with a history of mental illness or long-term use of psychotropic drugs (dementia, schizophrenia), chronic analgesic drug use, alcoholism, and cognitive impairment
4. Any cardiovascular or cerebrovascular accidents occurred within 3 months, such as myocardial infarction, stroke, transient ischemic attack
5. Myasthenia gravis patients
6. Unable to cooperate to complete the test, the patient or family member rejected the participant
65 Years
ALL
No
Sponsors
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Second Affiliated Hospital of Nanchang University
OTHER
Responsible Party
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Fuzhou Hua
Chief Physician
Locations
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the Second Affiliated Hospital of Nanchang University, Nanchang University
Nanchang, Jiangxi, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2023-OB-01
Identifier Type: -
Identifier Source: org_study_id
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