Thromboelastography (TEG) and Clopidogrel Withdrawal Time in Elderly Patients With Hip Fracture
Primary Purpose
Hip Fracture
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Thrombelastograph and surgical timing
Sponsored by
About this trial
This is an interventional treatment trial for Hip Fracture focused on measuring Hip Fracture, Clopidogrel, Withdrawal, surgical timing, Thromboelastogram
Eligibility Criteria
Inclusion Criteria:
- hip fracture and operation
- taking clopidogrel for more than one week before injury, with or without taking aspirin at the same time
Exclusion Criteria:
- high energy injury (such as traffic accident, falling from height), bilateral hip fracture, multiple fractures or injuries, pathological fracture
- malignant tumor patients
- hormone users
- patients with recent active bleeding or bleeding ulcer
- primary or secondary coagulation dysfunction or depression caused by other reasons than taking antiplatelet drugs (for example, taking warfarin)
- patients with other acute or unstable diseases requiring delayed surgery (acute heart failure, myocardial infarction, cerebral infarction, cerebral hemorrhage, severe pulmonary infection, deep vein thrombosis or pulmonary embolism, etc.)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
TEG group
Non-TEG group
Arm Description
Outcomes
Primary Outcome Measures
Estimated red blood cell loss
The amount of red blood cell loss estimated by blood routine changes
Secondary Outcome Measures
Blood transfusion
Red blood cell infusion volume
Full Information
NCT ID
NCT04165538
First Posted
October 16, 2019
Last Updated
November 14, 2019
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
1. Study Identification
Unique Protocol Identification Number
NCT04165538
Brief Title
Thromboelastography (TEG) and Clopidogrel Withdrawal Time in Elderly Patients With Hip Fracture
Official Title
Safety and Effectiveness of Clopidogrel Withdrawal Time Guided by Thromboelastography in Elderly Patients With Hip Fracture
Study Type
Interventional
2. Study Status
Record Verification Date
October 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 2020 (Anticipated)
Primary Completion Date
January 2022 (Anticipated)
Study Completion Date
January 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In the elderly patients with hip fracture, some often take antiplatelet drugs such as clopidogrel due to the ischemic cardiovascular or cerebrovascular diseases. In traditional practice, these patients often need to stop medication for 5-7 days before surgery. But on the other hand, delayed surgery will lead to a significant increase in fracture related complications. Therefore, the appropriate time for drug withdrawal is particularly important in this population.
Thromboelastography is a monitoring method that can accurately judge the anticoagulation status of patients. We hope to use thromboelastography to guide the time of drug withdrawal, shorten the time of drug withdrawal as much as possible, and reduce the incidence of fracture related complications without increasing the risk of massive hemorrhage.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Fracture
Keywords
Hip Fracture, Clopidogrel, Withdrawal, surgical timing, Thromboelastogram
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
140 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
TEG group
Arm Type
Experimental
Arm Title
Non-TEG group
Arm Type
No Intervention
Intervention Type
Procedure
Intervention Name(s)
Thrombelastograph and surgical timing
Intervention Description
Patients in the TEG group will undergo a Thrombelastograph test after admission, and the timing of operation will be determined according to the results of the test, that is, 1 day, 3 days and 5 days later respectively for patients with ADP-induced platelet-fibrin clot strength (MAADP) of > 50 mm, 30-50 mm and < 30 mm. For Non-TEG patients, the drug withdrawal time is determined by the doctor in charge according to the clinical routine, generally about one week.
Primary Outcome Measure Information:
Title
Estimated red blood cell loss
Description
The amount of red blood cell loss estimated by blood routine changes
Time Frame
From admission when the first blood routine will be obtained to discharge when the last blood routine will be obtained, up to postoperative day 7.
Secondary Outcome Measure Information:
Title
Blood transfusion
Description
Red blood cell infusion volume
Time Frame
From admission when the first blood routine will be obtained to discharge when the last blood routine will be obtained, up to postoperative day 7.
Other Pre-specified Outcome Measures:
Title
Length of stay
Description
Total length of stay
Time Frame
from admission to discharge,up to one year after operation
Title
Mortality
Description
One year all-cause mortality
Time Frame
within one year after operation
Title
Cerebrovascular accident
Description
Ischemic brain disease
Time Frame
within one year after operation
Title
Acute coronary syndrome
Description
Ischemic heart disease
Time Frame
within one year after operation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
hip fracture and operation
taking clopidogrel for more than one week before injury, with or without taking aspirin at the same time
Exclusion Criteria:
high energy injury (such as traffic accident, falling from height), bilateral hip fracture, multiple fractures or injuries, pathological fracture
malignant tumor patients
hormone users
patients with recent active bleeding or bleeding ulcer
primary or secondary coagulation dysfunction or depression caused by other reasons than taking antiplatelet drugs (for example, taking warfarin)
patients with other acute or unstable diseases requiring delayed surgery (acute heart failure, myocardial infarction, cerebral infarction, cerebral hemorrhage, severe pulmonary infection, deep vein thrombosis or pulmonary embolism, etc.)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Min Yan, Doctor
Phone
+86-13757118632
Email
zryanmin@zju.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Min Yan, Doctor
Organizational Affiliation
Zhejiang University
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
Yes
Learn more about this trial
Thromboelastography (TEG) and Clopidogrel Withdrawal Time in Elderly Patients With Hip Fracture
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