Overview

Intravenous Versus Topical Administration of Low Dose Epinephrine Plus Combined Administration of Intravenous and Topical Tranexamic Acid (TXA)for Primary Total Knee Arthroplasty

Status:
Unknown status
Trial end date:
2017-07-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to compare the blood loss of intravenous and topical administration of low dose epinephrine plus combined administration of intravenous and topical tranexamic acid for primary total knee arthroplasty.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Southwest Hospital, China
Treatments:
Epinephrine
Epinephryl borate
Racepinephrine
Tranexamic Acid
Criteria
Inclusion Criteria:

- All patients between the ages of 20 and 75 who were diagnosed with osteoarthritis of
the knee and scheduled for an elective primary total knee arthroplasty and those who
were willing and able to return for follow-up over at least a 6-month postoperative
period

Exclusion Criteria:

- Acute coronary syndrome < 6 months

- Glaucoma,pheochromocytoma, thyrotoxicosis, digoxin intoxication, serum potassium < 3.0
mmol, alcohol abuse, premenopausal women

- Current treatment with adenosine diphosphate (ADP) receptor antagonists, Factor Xa or
thrombin inhibitors,heparin (excluding Low Molecular Weight Heparin (LMWH) for
perioperative thromboprophylaxis), tricyclic antidepressants, or monoamine
oxidase(MAO) or Catechol-O-methyltransferase (COMT) inhibitors

- Patients with history of thromboembolic disease, bleeding disorder

- Patients with history of renal impairment, cardiovascular diseases (previous
myocardial infarction, atrial fibrillation) or cerebrovascular conditions (previous
stroke or peripheral vascular surgery)

- Allergy to TXA