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Blood Transfusion Among Patients With Pelvic Fracture in China

Establishment for Prediction Model of Intraoperative Blood Transfusion for Patients With Pelvic Fracture in China: A Multicenter Observational Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03855644
Acronym
PBM
Enrollment
2000
Registered
2019-02-27
Start date
2019-04-05
Completion date
2019-09-01
Last updated
2019-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Transfusion Complication, Pelvic Fracture, Transfusion Reaction

Keywords

Pelvic Fracture, Predictive Model, Blood Transfusion, Perioperative period

Brief summary

According to the patient's blood management concept, this study intends to collect basic information, surgical data, blood transfusion related data and patient prognosis data of patients with pelvic fractures, and to construct a predictive model of intraoperative blood transfusion in patients with pelvic fractures by multiple linear regression analysis. To guide physicians use blood accurately during surgery. Prompt doctors to reduce blood transfusion dose and improve patient prognosis by stopping bleeding and blood recovery before surgery.

Detailed description

2.1 Research Objectives: This study aims to construct a blood transfusion model for pelvic fractures, to guide the rational use of blood during surgery, and to improve the prognosis of patients. 2.2 Research content: 2.2.1 Collect basic data, surgical data, blood transfusion related data and patient prognosis related data of patients with pelvic fractures. 2.2.2 Gradually incorporate and exclude data from multiple linear regression models. 2.2.3 Verify the specificity and sensitivity of the intraoperative blood transfusion prediction model. 2.2.4 Create a visualization window to guide clinical blood. 2.2.5 Put into clinical trial and feedback, and continue to verify 2.3 Key issues to be resolved 2.3.1 The factors related to intraoperative blood transfusion in patients with pelvic fractures (such as blood oxygenation, blood loss, HB value, intraoperative autologous blood recovery, blood pressure, heart rate, etc.) were initially screened by univariate analysis. 2.3.2 Reasonably standardize the objective and subjective indicators of different units and different institutions. 2.4 Expected research results Intraoperative blood transfusion prediction model and window for patients with pelvic fractures. 2.5 Assessment indicators Published 1-2 papers. Create a visual applet and put it into trial.

Interventions

None listed

Sponsors

Beijing Shijitan Hospital, Capital Medical University
CollaboratorOTHER
The Affiliated Hospital Of Southwest Medical University
CollaboratorOTHER
Zhejiang Provincial People's Hospital
CollaboratorOTHER
Central South University
CollaboratorOTHER
Qilu Hospital of Shandong University
CollaboratorOTHER
Beijing Aerospace General Hospital
CollaboratorOTHER
The Third Xiangya Hospital of Central South University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
1 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* (1) 1\<Age\<80, and Chinese residents living in China more than 3 years; * (2) Hemoglobin value less than 100g/L during hospitalization;

Exclusion criteria

* (1) Participants who suffered from pelvic fracture within 3 months * (2) Participants who suffer from pathological fractures of the pelvis caused by malignant tumors * (3) Participants with chronic anemia and coagulopathy * (4) Participants who rufuse blood transfusion

Design outcomes

Primary

MeasureTime frameDescription
Matta Radiographic Scoring6 months of postoperationReductions were graded by the maximal displacement measured on the 3 standard views of the pelvis. Criteria were: excellent 4 mm or less, good 5 to 10 mm, fair 10 to 20 mm, and poor more than 20 mm.
Mortality24 hours after the Patients' HospitalizationMortality during hospitalization

Secondary

MeasureTime frameDescription
Hb difference24 hours after transfusionHb difference before and after transfusion
Pain assessed by the VAS15 minutes, 30 minutes, 1 hours, 2 hours, 4 hours, 6 hours, 12 hours, 18 hours, 24 hours postoperativelyChange in the Pain Intensity Score (0-10 NRS)
Postoperative Duration of Stay in Hospital of patients52 WeeksThe postoperative duration of stay in hospital of patients between the restrictive transfusion group and the liberal transfusion group are compared.

Countries

China

Contacts

Primary ContactRong Gui, Ph.D
aguirong@163.com13975199279
Backup ContactHuang Xueyuan, Mater degree
2458481936@qq.com15273157184

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026