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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05530161
Other study ID # 2020-822
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2015
Est. completion date September 1, 2023

Study information

Verified date August 2022
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact yongan xu, doctor
Phone 13757164833
Email xuyongan2000@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hypocalcaemia is an independent risk factor of TIC in elderly trauma patients. TIC combined with hypocalcemia had worse coagulation function and more serious acidosis.


Description:

This 5-year retrospective, observational, single-center study was conducted at the Second Affiliated Hospital of Zhejiang University Medical School (SAHZU, China). Elderly patients with trauma were registered when they were admitted into intensive care unit affiliated to department of Emergency medicine (EICU) since January 2015 and September 2020.The purpose of this study is to elucidate the effect of hypocalcemia on TIC in elderly trauma patients through a single-center retrospective study, so as to further optimize the diagnosis and treatment strategies for TIC in elderly trauma patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 371
Est. completion date September 1, 2023
Est. primary completion date September 1, 2023
Accepts healthy volunteers No
Gender All
Age group 65 Years to 100 Years
Eligibility Inclusion Criteria: - age=65 years old - history of trauma Exclusion Criteria: - previous anticoagulants or antiplatelet medication; - Coagulopathy caused by previous underlying diseases; - Blood products transfused before admission; - Cardiac arrest on admission; - Malignant tumor; - Data incomplete

Study Design


Intervention

Other:
hypocalcemia
hypocalcemia or normocalcemia

Locations

Country Name City State
China SAHZU Hanzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Internationalized Normalized Ratio (INR) coagulation function :Internationalized Normalized Ratio (INR) 24 hour
Primary Activated Partial Thromboplastin Time (APTT) coagulation function : Activated Partial Thromboplastin Time (APTT) 24 hour
Primary Prothrombin Time (PT) coagulation function : Prothrombin Time (PT) 24 hour
Secondary Blood products rate the rate of Blood products use through study completion, an average of 1 week
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