To Establish a Blood Transfusion Prediction Model for Liver Transplantation Patients Based on PBM
To Establish a Prediction Model of Massive Blood Transfusion for Liver Transplantation Patients Based on Patient Blood Management
1 other identifier
observational
2,000
1 country
1
Brief Summary
Based on the principle of patient blood management, this study aims to reduce the risk of blood transfusion in allogeneic liver transplantation patients, to ensure the safety of blood transfusion, and to provide new methods and basis for restrictive blood transfusion.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2019
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 20, 2019
CompletedFirst Posted
Study publicly available on registry
January 24, 2019
CompletedStudy Start
First participant enrolled
March 20, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2021
CompletedFebruary 21, 2019
February 1, 2019
9 months
January 20, 2019
February 20, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
one year mortality
All-cause mortality
2019-2021
Secondary Outcomes (1)
Intraoperative blood transfusion
2019-2021
Study Arms (1)
Liver transplant
1. 18 years to 65 2. 48h preoperative biochemical indicators, blood general indicators, coagulation test complete
Interventions
Eligibility Criteria
Allogeneic liver transplantation surgery
You may qualify if:
- h preoperative biochemical indicators, blood general indicators, coagulation test complete
You may not qualify if:
- \. Inspection information is not detailed 2. Blood transfusion information is not detailed 3.Postoperative medical record information is not detailed
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- The Third Xiangya Hospital of Central South Universitylead
- Second Xiangya Hospital of Central South Universitycollaborator
- RenJi Hospitalcollaborator
- Qilu Hospital of Shandong Universitycollaborator
Study Sites (1)
the Third Xiangya Hospital of Central South University
Changsha, Hunan, 410006, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 2 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 20, 2019
First Posted
January 24, 2019
Study Start
March 20, 2019
Primary Completion
December 1, 2019
Study Completion
December 31, 2021
Last Updated
February 21, 2019
Record last verified: 2019-02