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Intravenous application of tranexamic acid and intravenous and oral combination enhanced recovery after surgery to reduce postoperative hidden hemorrhage and inflammatory reaction-a prospective randomized controlled trial

Intravenous application of tranexamic acid and intravenous and oral combination enhanced recovery after surgery to reduce postoperative hidden hemorrhage and inflammatory reaction-a prospective randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16009770
Enrollment
Unknown
Registered
2016-11-08
Start date
2016-11-08
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

Hip osteoarthritis and avascular necrosis of the femoral head, hip dysplasia

Interventions

Intravenous group:The intravenous application of tranexamic acid
Combined intravenous and oral group:Combined intravenous and oral application of tranexamic acid

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Patients following primary total hip arthroplasty due to osteoarthritis, hip dysplasia and ischemic necrosis of the femoral head; (2) Patinets with preoperative platelet and coagulation function dysfunction; (3) Preoperative double lower limb venous color Doppler ultrasound was not abnormal; (4) voluntarily participated in clinical trials and signed informed consent, good compliance of patients.

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

Design outcomes

Primary

MeasureTime frame
Hidden blood loss;Inflammatory index;D-Dimer;Fibrin degradation products;

Secondary

MeasureTime frame
The drop of hemoglobin;Allogeneic blood transfusion rate;Total blood loss;VAS;Limb swelling ratio;Joint mobility;Postoperative hospital stay;

Countries

China

Contacts

Public ContactFuxing Pei

West China Hospital, Sichuan University

peifuxinghuaxi@163.com+86 18980601380

Outcome results

None listed

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