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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03044041
Other study ID # OrthoTU08
Secondary ID
Status Completed
Phase Phase 4
First received January 29, 2017
Last updated January 27, 2018
Start date January 2016
Est. completion date June 2017

Study information

Verified date January 2018
Source Thammasat University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare blood loss between using low dose (500 mg) and high dose (3 g) topical intra-articular tranexamic acid after total knee arthroplasty in double-blind RCT


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date June 2017
Est. primary completion date January 2017
Accepts healthy volunteers No
Gender All
Age group 50 Years to 90 Years
Eligibility Inclusion Criteria:

- Osteoarthritic knee who underwent primary total knee arthroplasty

Exclusion Criteria:

- Abnormal coagulation or bleeding disorder

- Allergy to tranexamic acid

- History of thromboembolism or ischemic heart disease or cerebrovascular accident

- chronic kidney disease stage 3-4

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tranexamic Acid
IA (intra-articular) tranexamic acid after capsule closure

Locations

Country Name City State
Thailand Thammasat University Klong Luang Pathum Thani

Sponsors (1)

Lead Sponsor Collaborator
Thammasat University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total blood loss Blood loos that calculated from Haemoglobin drop at 72 hours after surgery 72 hours after TKA
Secondary Blood transfusion incidence of blood transfusion after surgery 0-72 hours after surgery
Secondary Rate of participants with thromboembolism Clinical thromboembolism after surgery At 72 hours and 2 weeks after surgery
Secondary Rate of participants with infection Superficial or deep infection after TKA 0-3 months after surgery
Secondary Knee ROM Range of motion of the knee At 2, 6 weeks after surgery
Secondary Functional score Modified WOMAC At 6 weeks after surgery
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