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Efficacy of tranexamic acid combined with Carbazochrome Sodium Sulfonate on blood loss in primary total knee arthroplasty : a prospective randomized controlled trial

Hemostasis management and fast rehabilitation for patients undergoing total knee arthroplaty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015839
Enrollment
Unknown
Registered
2018-04-24
Start date
2018-05-04
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

osteoarthritis

Interventions

Group 2:Tranexamic acid ( intravenous injection) + Carbazochrome Sodium Sulfonate ( intravenous injection)
Group 3:Tranexamic acid ( intravenous injection) + Carbazochrome Sodium Sulfonate (Infiltration of the surrounding tissue of the capsule )
Group 4:Tranexamic acid ( intravenous injection)

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. patients with osteoarthritis and have to undergo TKA; 2. BMI: 20-35 kg/m2; 3. American Society of Anesthesiologists degree before operation: I~III grades; 4. Aged 18 years old and above;

Exclusion criteria

Exclusion criteria: 1. of tranexamic acid sodium and card collaterals, narcotic drug allergy; 2. the art side of the knee joint deformities (> 20 degree flexion deformity; Varus and valgus deformity > 20 degree) and joint rigidity; 3. An alcoholic or pregnant person; Use anticoagulants or contraceptives 5 days before surgery; 4. Repair part or total knee replacement, secondary osteoarthritis (rheumatoid arthritis, suppurative arthritis or post-traumatic arthritis); 5. The history of thromboembolic disease (DVT), pulmonary embolism (PE), coagulopathy, recent arterial thromboembolic events (such as myocardial infarction or stroke), hypercoagulability, hemophilia; 6. Severe cardiovascular and respiratory diseases; Kidney and liver failure, kidney transplantation history; 7. A person who refuses to participate in or refuse to accept blood products.

Design outcomes

Primary

MeasureTime frame
total blood loss;haemoglobin;haematocrit;reduction in haemoglobin concentration;D-dimer;

Secondary

MeasureTime frame
transfusion rates;thromboelastogram;inflammatory cytokines;range of motion of the knee;

Countries

China

Contacts

Public ContactPengde Kang

West China Hospital, Sichuan University

m13880025417@163.com+86 28 85422426

Outcome results

None listed

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