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
NA
600 participants
INTERVENTIONAL
2019-10-01
2027-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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ERAS group
the patients accepting eras nursing protocol ;
ERAS nursing
Patients were given education before surgery, fluid and anesthetic drug management during surgery, early ambulation, fluid management and early feeding after surgery, etc
non-eras group
the patients not accepting eras nursing protocol ;
non eras nursing
Patients were under the routine management without eras protocol
Interventions
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ERAS nursing
Patients were given education before surgery, fluid and anesthetic drug management during surgery, early ambulation, fluid management and early feeding after surgery, etc
non eras nursing
Patients were under the routine management without eras protocol
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
Surgery intensive care, unable to cooperate (language
Speech disorders, psychopathology)
18 Years
85 Years
ALL
Yes
Sponsors
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The Second Hospital of Shandong University
OTHER
Responsible Party
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Locations
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The second hospital of shandong university
Jinan, Shandong, China
Countries
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Central Contacts
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Hongju Wang
Role: CONTACT
Facility Contacts
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Other Identifiers
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ERAS (PRO)-based study
Identifier Type: -
Identifier Source: org_study_id
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