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NCT Number: NCT05504577

Kaolin-based Hemostatic Gauze in Total Knee Arthroplasty

This study is to conduct a prospective randomized controlled trial to investigate the blood-conservation effect of combination of intravenous TXA and QCG in a primary TKA procedure.

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Key information

Age range

50 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Kaohsiung Chang Gung Memorial Hospital

Kaohsiung, Taiwan

About this study

Total knee arthroplasty (TKA) is associated with considerable blood loss and increasing needs for allogenic blood transfusion. Previous studies demonstrated a transfusion rates ranging from 10% to 38% after standard TKAs. Tranexamic acid (TXA), an inhibitor of fibrinolysis, was reportedly effective reducing blood loss after standard TKA. Our previous experiences in minimally invasive (MIS) TKA showed that intraoperative intravenous infusion of TXA reduced 45% of postoperative blood loss and needs for transfusion from 20% to 4%. Our study demonstrated that an equal efficacy of intraarticular topical TXA in blood conservation compared with intravenous infusion of TXA.

In addition to TXA, the Quikclot sponge (QCG; Z-Medica, Wallingford, CT, USA) is a newly developed hemostatic agent employing an inorganic mineral (kaolin). The QCG has predominantly been used in combat settings and trauma surgery. Recently, the application of QCG in interventional procedures, and non-orthopedic surgeries was reported. Literature describing the use of QCG as an alternative approach to achieve hemostasis in the field of orthopedics is limited. There is no study to investigate the blood-saving effect of QCG in a TKA procedure, especially in combined with TKA. Therefore we conduct the study to understand the efficacy of this sponge on blood conservation in TKA We believe that combination with the two different mechanism of blood-conservation agents can bring a synergistic effect in blood saving after TKA. Our purpose of this study therefore is to conduct a prospective randomized controlled trial to investigate the blood-conservation effect of QCG combined with TXA use.

Material and Methods:

Based on our previous clinical research, the mean TBL among patients receiving intravenous TXA was 921 mL, with a standard deviation of 259 mL. The sample-size calculation was based on the prespecified comparison between the QCG and control groups, assuming a clinically meaningful difference of 200 mL, a two-sided alpha level of 0.05, and a statistical power of 95%. Using one-way ANOVA test in G*Power (version 3.1.9.4), a minimum of 44 patients per group was required. To account for potential attrition, 140 patients will be enrolled.

The first group will be treated by application of QCG in joint space and TXA 1g intravenous injection before tourniquet deflation. The second group will be treated by application of normal gauze in joint space and TXA 1g intravenous injection before tourniquet deflation. The third group will be treated only TXA 1g intravenously injection alone before tourniquet deflation. We will observe whether there is difference in the blood-conservation effect by total blood loss calculation, hemoglobin loss and transfusion requirement between these three groups. Besides, any complications including VTE, deep infection, wound complications within postoperative 3 months will be recorded.

Study years: one year

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with advanced osteoarthritis of the knee and undergo primary unilateral minimally invasive TKA
  • Age > 50 years and < 90 years
  • Failure of medical treatment or rehabilitation
  • Hemoglobin ≧ 11g/dl
  • No use of non-steroid anti-inflammatory agent, antiplatelets or anticoagulants at least 3 days before operation

Exclusion criteria

  • Preoperative Hemoglobin <11 g/dl
  • History of infection or intraarticular fracture of the affective knee
  • Renal function deficiency (GFR <30 ml/min/1.73m2)
  • Elevated liver enzyme (AST/ALT level are more than twice normal range) , history of liver cirrhosis, impaired liver function(elevated total bilirubin level) and coagulopathy (including long-term use anticoagulant)
  • History of deep vein thrombosis, ischemic heart disease or stroke, in which life-long oral anticoagulant are required.
  • Contraindications of tranexamic acid, or rivaroxaban
  • Allergy to tranexamic acid, kaolin, rivaroxaban, or the excipients
  • History of heparin-induced thrombocytopenia (HIT)
  • Coagulopathy or bleeding tendency caused by organ dysfunction, such as cirrhosis, bone marrow suppression etc.
  • Patient who have active bleeding disorder, such as intracranial hemorrhage, upper GI bleeding, hematuria..

Treatment and study plan

Tranexamic acid injection

Drug

Tranexamic acid 1g is intravenously injected at 10 mins before tourniquet deflation. .

Other names: transamine injection

apply the QCG

Device

apply the QCG (Quikclot Z-fold hemostatic gauze, Z-Medica, Wallingford, CT, USA) into the joint space. Compress the knee joint by elastic bandage. Compress the knee joint by elastic bandage. Deflate the tourniquet for 10 minutes

apply surgical gauze

Device

apply the normal surgical gauze into the joint space. Compress the knee joint by elastic bandage. Deflate the tourniquet for 10 minutes

Primary outcomes

  1. Total Blood Loss

    Time frame: Preoperative day to postoperative day 4

    The total blood loss was calculated according to Nadler et al, which uses maximum postoperative decrease of the Hb level adjusted for weight and height of the patient. Total blood loss consists of amount of blood loss calculated from the maximum Hb loss and amount of blood transfused

Secondary outcomes

  1. Blood transfusion rate

    Time frame: To three months after operation

    We will record the event of blood transfusion, and calculate the incidence of transfusion

  2. All symptomatic thrombotic events including deep vein thrombosis, pulmonary embolism

    Time frame: To three months after operation

    We will record all symptomatic thrombotic events including deep vein thrombosis, pulmonary embolism in our study, and calculate the incidence of them

Sponsors and collaborators

Lead sponsor

Chang Gung Memorial Hospital

Other

Registry information

Official study title

Blood-saving Effect of Kaolin-based Hemostatic Gauze Combined With Intravenous Tranexamic Acid in Total Knee Arthroplasty

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Aug 17, 2022
Registry last updated
Jul 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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