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Efficacy of Tranexamic Acid combined with Carbazochrome Sodium Sulfonate on blood loss in primary total hip arthroplasty using a direct anterior approach: a prospective randomized controlled trial

Evaluation of safety and efficacy of arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020498
Enrollment
Unknown
Registered
2019-01-02
Start date
2019-01-04
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

osteoarthritis or Osteonecrosis of femoral head

Interventions

Group A:Tranexamic acid (intravenous) + Carbazochrome sodium sulfonate(infiltration around joint capsule)
Group B:Tranexamic acid (intravenous)

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. patients with osteoarthritis or osteonecrosis of the femoral head (Ficat III?IV) and have to undergo THA; 2. BMI 20-35 kg/m2; 3. American Society of Anesthesiologists grade I to III.

Exclusion criteria

Exclusion criteria: 1. The patients with anaphylactic acid, sodium carboxylic acid, anaesthesia drug allergy; 2. have a rigid hip joint, severe femoral deformity; 3. The posterior wall of the acetabulum was removed, and there was a history of surgery in the posterior hip; 4. The osteoarthritis (Crowe type 3 or 4) of DDH; 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. Persons who refuse to participate in or refuse to accept blood products.

Design outcomes

Primary

MeasureTime frame
total blood loss;haematocrit and haemoglobin (HB);reduction in haemoglobin concentration;transfusion rates;

Secondary

MeasureTime frame
intra-operative blood loss;Length of postoperative hospital stay;conglomeration parameter;

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