Skip to content

Peri-articular tranexamic acid injection in total knee/hip arthroplasty: a prospective randomized controlled trial

Peri-articular tranexamic acid injection in total knee/hip arthroplasty: a prospective randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16010270
Enrollment
Unknown
Registered
2016-12-27
Start date
2016-12-31
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

End-stage hip and knee joint disease

Interventions

A:Intravenous use of 15mg / kg tranexamic acid
B:Periarticular injection of 15mg / kg tranexamic acid

Sponsors

Orthopeadic Department,Peking Union Medical College Hospital,Chinese Academy of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients plan to receive total hip or total knee arthroplasty due to end-stage hip and knee joint disease

Exclusion criteria

Exclusion criteria: (1) Patinets with history of venous thromboembolism, pulmonary embolism, cerebral infarction, coronary heart disease; (2) Patients with coagulation disorders; (3) Anticoagulant drugs are being used; (4) Administration of NSAID for less than 1 weeks; (5) TXA allergy; (6) Severe liver and renal insufficiency; (7) Patients with high risk of thrombosis, including atrial fibrillation, cardiac pacemaker, and stent implantation; (8) severe hip and knee deformity.

Design outcomes

Primary

MeasureTime frame
blood loss;other safety indexes;

Secondary

MeasureTime frame
hidden blood loss;Inflammatory index;Drainage volume;complications;postoperative days required to straight leg elevation ;Thigh circumference;postoperative days required to stand ;

Countries

China

Contacts

Public ContactWENG Xisheng

Orthopedic Department, Peking Union Medical College Hospital,Chinese Academy of Medical Science

xshweng@medmail.com.cn+86 13366200018

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 14, 2026