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The effects of multiple doses of intravenous tranexamic acid on postoperative blood loss, inflammation, coagulation, fibrinolysis, and knee function in patients with gouty knee arthritis undergoing arthroscopic debridement

The effects of multiple doses of intravenous tranexamic acid on postoperative blood loss, inflammation, coagulation, fibrinolysis, and knee function in patients with gouty knee arthritis undergoing arthroscopic debridement

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032046
Enrollment
Unknown
Registered
2020-04-18
Start date
2020-04-16
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

knee gouty arthritis

Interventions

C:20mg/kgTXA before tourniquet release, intravenously (1 g TXA 3 h postoperatively

Sponsors

Department of Orthopaedic Surgery, West China Hospital, West China Medical School, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with gouty knee arthritis who underwent debridement under the microscope; 2. Patients with normal platelet and coagulation function before operation; 3. Those patients who had no abnormality in color Doppler ultrasonography of the veins of both lower limbs before operation; 4. Patients who voluntarily participate in the clinical trial and are willing to sign the informed consent and have good compliance.

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrolled systemic infection such as pulmonary infection and urinary tract infection before operation; 2. Patients with abnormal immune function or immune related diseases before operation; 3. Patients with abnormal preoperative inflammatory index (CRP > 20 mg / L); 4. Patients with abnormal preoperative fibrinolysis index (FDP > 5 mg / L); 5. Patients who took anticoagulants or aspirin for less than 1 week; 6. Patients who are allergic to tranexamic acid or have contraindications; 7. Patients at high risk of thrombosis, including AF, pacemaker and stent implantation; 8. Patients with history of venous thromboembolism, pulmonary embolism, cerebral infarction and coronary heart disease; 9. Patients with severe hepatorenal insufficiency.

Design outcomes

Primary

MeasureTime frame
Blood loss;ESR, CRP, IL-6, IL-10;D-dimmer;Fibrinogen Kinetics;

Secondary

MeasureTime frame
Hb;HCT;DVT, PE;Transfusion;Swelling;VAS pain score;color Doppler Ultrasonic (CDU) examination in lower extremity;ROM;Muscle strength;Drainage;Satisfaction scores;Sleep quality;

Countries

China

Contacts

Public ContactJian Li

West China Hospital, Sichuan University

18980601388@163.com+86 18980601388

Outcome results

None listed

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