Home › Pain After Surgery › NCT06479161
Effects of Oral Tranexamic Acid Following Total Knee Arthroplasty
Effects of Oral Tranexamic Acid Following Total Knee Arthroplasty on Postoperative Pain and Range of Motion: A Randomized Control Trial
Who can join
Ages 18 to 89 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * \- All patients undergoing either manual or robotic primary total knee arthroplasty (TKA) * Performed by participating Connecticut Joint Replacement Institute (CJRI) surgeons (Dr. Matthew Grosso, Dr. Robert McAllister, Dr. Chad Daniel, Dr. Eric Silverstein, Dr. Alex Dukas, Dr. Michael Joyce, Dr. Brett Wasserlauf). * Male and female patient age 18-89 * Primary diagnosis of knee osteoarthritis Exclusion Criteria: * Revision TKA * No exclusion based on gender * Patients \<18 and \>89 years old * Exclusion for IV oral tranexamic acid (TXA): * TXA allergy - there are NO absolute contraindications for TXA use. * History of stent placed within one year of surgery - patient will receive topical TXA as an alternative. * Exclusion for oral TXA: o Actively treated cancer or deep vein thrombosis (DVT) * Chronic opioid use (opioid use within the 4 weeks prior to surgery) * Allergies to nonsteroidal Anti-inflammatory drugs (NSAIDs) and acetaminophen * Patients with clinically significant drug interactions * Pre-existing neuropathy * Current or previous venous thrombosis (DVT or venous stasis disease) * Immuno-compromised secondary to medical condition * Immune-suppressive medications, chemotherapy * Pregnancy, breast feeding * History of pain catastrophizing. Major depressive disorder * History of suspected or known addiction to or abuse of illicit drug(s), prescription medicine(s), or alcohol within the past 2 years. * Currently on a neuroleptic agent \[e.g., gabapentin, pregabalin (Lyrica), duloxetine (Cymbalta) etc.\]. * Non-English speaking and reading patient populations * Any clinically significant event or condition uncovered during the surgery (e.g., excessive bleeding, acute sepsis) that, in the opinion of the investigator, renders the subject medically unstable or complicates the subject's post-operative course.
About the study
The primary purpose of this study is to evaluate postoperative pain. Secondary outcomes evaluated in this study will include range of motion (ROM), opioid consumption, and ambulation. Each outcome measure will be evaluated, oral tranexamic acid (TXA) in the experiment arm and placebo in the control arm, after total knee arthroplasty (TKA) at postoperative days 0-3, and weeks 1, 2, 6, and 12.
What is being tested
- Tranexamic acid (drug)
Sponsor: Matthew Grosso, MD · Participants: 80 · Started: Jun 10, 2024
Contact the study team
- Gina Panek, BS · Phone: 860-714-4164
- Czarina Weinz · Phone: 860-714-0467
Official record on ClinicalTrials.gov — NCT06479161
Locations in the U.S.
| Connecticut | Trinity Health Of New England/CT Joint Replacement Institute, Hartford |
Conditions
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.