Establishment and Validation of Early-warning Model of Perioperative Pain for the Elders
NCT ID: NCT04228705
Last Updated: 2020-01-14
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
6000 participants
OBSERVATIONAL
2019-12-13
2020-12-12
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
Study Groups
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The elders
Patients aged over 59 years old
No interventions assigned to this group
The young adults
Patients aged from 18 to 59 years old
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Undergoing general or regional anesthesia
* Hospitalized for at least 24 hours after surgery
* Able to give informed consent
* Able to read and write
Exclusion Criteria
* A history of substance abuse
* Admitted to ICU after surgery
* Patients with advanced tumors who have received preoperative chemotherapy or who are expected to receive postoperative chemotherapy.
18 Years
ALL
No
Sponsors
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Chinese PLA General Hospital
OTHER
First Affiliated Hospital of Guangxi Medical University
OTHER
Zhejiang University
OTHER
Peking University People's Hospital
OTHER
Responsible Party
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Yi Feng, MD
Director of department of anesthesiology and pain management
Principal Investigators
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Feng Yi, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Peking University People's Hospital
Locations
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Peking University People's Hospital
Beijing, Beijing 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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2019PHB258-01
Identifier Type: -
Identifier Source: org_study_id
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