Perioperative Blood Transfusion and Increased One-year Mortality
NCT ID: NCT07094295
Last Updated: 2025-07-30
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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COMPLETED
97443 participants
OBSERVATIONAL
2012-01-01
2016-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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PBT group
Patients in PBT group received red blood cell concentrate units during surgery and up to one month postoperatively.
perioperative blood transfusion
The PBT group received the red blood cell concentrate units during surgery and up to one month postoperatively.
No-PBT group
Patients in No-PBT group did not receive red blood cell concentrate units during surgery and up to one month postoperatively.
No interventions assigned to this group
Interventions
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perioperative blood transfusion
The PBT group received the red blood cell concentrate units during surgery and up to one month postoperatively.
Eligibility Criteria
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Inclusion Criteria
* Patients undergoing first-time cardiothoracic surgery, orthopedics, obstetrics and gynecology, general surgery, otolaryngology, hand surgery, neurosurgery, colorectal surgery, urology, plastic surgery, and oral and maxillofacial surgery were included.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Changhai Hospital
OTHER
Responsible Party
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Wen-bin Lu, MD
Principal Investigator
Other Identifiers
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PBTOM
Identifier Type: -
Identifier Source: org_study_id
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