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Clinical Trials/CTRI/2017/07/009076
CTRI/2017/07/009076
Completed
未知

The comparative Efficacy and Safety of Topical and Intravenous Tranexamic acid for Reducing Perioperative Blood Loss in Total Knee Arthroplasty- A Randomized Controlled Non-inferiority Trial

SUNSHINE HOSPITALS0 sites113 target enrollmentTBD
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ConditionsHealth Condition 1: null- Primary Osteoarthritis Knee

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Primary Osteoarthritis Knee
Sponsor
SUNSHINE HOSPITALS
Enrollment
113
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
April 28, 2017
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •1\. All patients undergoing total knee arthroplasty for primary
  • •arthroplasty knee
  • •2\.Patients who are willing to participate in the study.
  • •3\.Patient without exclusion criteria.

Exclusion Criteria

  • •1\.Allergy to the TXA
  • •2\.H/O Coagulopathy,abnormal PT or APTT
  • •3\.Past H/O Thromboembolic event
  • •4\.Treatment with Aspirin or NSAIDS in the last week
  • •5\.plasma creatinine \> 115 micro moles /litre for males
  • •And \>100 micro moles/litre in females.
  • •6\.Acute infection\[eg;leukocytosis or fever]
  • •7\.Malignancy
  • •8\.MI in preceding 12 months,unstable angina
  • •9\.Patient who were given plasma in perioperative period

Outcomes

Primary Outcomes

Not specified

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