Skip to content

Efficacy and safety of intraoperative intravenous and intraarticular tranexamic acid combined with oral tranexamic acid for perioperative blood loss and fibrinolysis in total knee arthroplasty

Intraoperative Intravenous and Intra-Articular Plus Postoperative oral Tranexamic Acid in Total Knee Arthroplasty

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033594
Enrollment
Unknown
Registered
2020-06-06
Start date
2020-06-05
Completion date
Unknown
Last updated
2020-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

osteoarthritis

Interventions

Group A:ntraoperative tranexamic acid (intravenous 1g+ intra-articular 1g) + postoperative oral administration of 3 doses of tranexamic acid (oral administration of 2gTXA at 2, 8 and 14h after surgery
Group B:Intraoperative tranexamic acid (intravenous 1g+ intra-articular 1g) + postoperative oral administration of 3 doses of tranexamic acid (oral 2g of placebo pills 2, 8 and 14h after surgery)

Sponsors

Department of Orthopedics, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as knee osteoarthritis requiring unilateral primary TKA surgery. 2. American Society of Anesthesiologists degree before operation: I~III grade. 3. Over 18 years of age.

Exclusion criteria

Exclusion criteria: 1. People who are allergic to tranexamic acid; 2. There was an operative knee deformity (buckling deformity > 20 degrees; Varus and valgus deformity BBB 0 20 degrees) and stiffness of joints; 3. Revision partial or total knee replacement, suppurative arthritis or post-traumatic arthritis; 4. Serious cardiovascular and respiratory diseases; Kidney and liver failure, history of kidney transplantation; 5. Refusing to participate in or accept blood products.

Design outcomes

Primary

MeasureTime frame
Perioperative blood loss or total blood loss;

Secondary

MeasureTime frame
Invisible blood loss;Intraoperative blood loss;Inflammatory markers;Fibrinolytic marker;range of motion;Blood transfusion rate (%);pain score;LOS(length of stay);

Countries

China

Contacts

Public ContactKang Pengde

Department of Orthopedics, West China Hospital, Sichuan University

kangpd@163.com+86 18980601953

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026