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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02867163
Other study ID # TXA in TKR
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 16, 2017
Est. completion date November 8, 2017

Study information

Verified date February 2019
Source University of New Mexico
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is an observational trial to estimate the incidence of deep vein thrombosis (DVT) in total knee replacement patients who received an intraoperative dose of tranexamic acid.


Description:

This study is anticipated to consist of 30 participants over 18 years of age scheduled for total knee arthroplasty at Sandoval Regional Medical Center with administered intraoperative tranexamic acid, who do not meet the exclusion criteria. The patients will be examined on postoperative day 1. Lower-extremity ultrasound will be used to screen for deep vein thrombosis (DVT). Incidence data for DVT will then be compared with the historical incidence rate at our institution for total knee arthroplasty without the use of tranexamic acid, which is approximately 12%. Patients found on screening to have deep vein thrombosis will be referred for appropriate care.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date November 8, 2017
Est. primary completion date November 8, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients scheduled for total knee arthroplasty at Sandoval Regional Medical Center with an intraoperative dose of tranexamic acid

Exclusion Criteria:

- Previous deep vein thrombosis or pulmonary embolism episode

- Known coronary artery disease or peripheral vascular disease

- Previously diagnosed hypercoagulable states (e.g. Leiden factor V, antiphospholipid antibody, protein C or S deficiency)

- Pregnancy

- Creatinine clearance less than 30 ml/min

- Non-fluency in English

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Tranexamic Acid
Intravenous or local administration of TXA, in any dosage

Locations

Country Name City State
United States Sandoval Regional Medical Center Rio Rancho New Mexico

Sponsors (1)

Lead Sponsor Collaborator
University of New Mexico

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Deep Vein Thrombosis Incidence of deep vein thrombosis diagnosed by ultrasound scan on postoperative day 1 One day
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