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This is a Study to Verify if Tranexamic Acid Can Reduce the Anemia After a Femoral Shaft Fractures Surgery (ORL-ORT-023)

Primary Purpose

Femoral Shaft Fracture

Status
Withdrawn
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Tranexamic Acid
Sponsored by
Christian Candrian
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Femoral Shaft Fracture

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Acute femoral shaft fracture.
  • Patients treated surgically with intramedullary nail or femoral plate
  • Patients aged 18-80 years old.
  • Patients with a BMI >18.5 and <35.
  • Patients able to provide informed consent and follow all the study procedures as indicated by the protocol.
  • Informed Consent as documented by signature

Exclusion Criteria:

  • Pathological fracture or other lower limb fractures associated or multiple fractures.
  • Use of any anticoagulant at the time of admission (eg, vitamin K antagonists, anti-thrombin agents, antiplatelet agents or factor IIa and Xa inhibitors).
  • Contraindications to TXA (eg documented allergy to TXA).
  • Hepatic dysfunction (aspartate transaminase (AST)/alanine transaminase (ALT)>60 U/l) or renal dysfunction (Cr >1.5 mg/dl of glomerular filtration rate (GFR)>30 ml/min).
  • History of DVT or pulmonary embolus.
  • Active coronary artery disease or cerebrovascular accident (event in the past 12 months).
  • Coagulopathy based on admission laboratory values (international normalised ratio (INR)>1.4, partial thromboplastin time (PTT)>1.4× normal sec, platelets <50 000 per mm3)
  • Women who are pregnant or breast feeding.
  • Known or suspected non-compliance, drug or alcohol abuse.
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant.
  • Participation in another study with investigational drug within the 30 days preceding and during the present study.
  • Previous enrolment into the current study.
  • Enrolment of the investigator, his/her family members, employees and other dependent persons.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    A: Tranexamic Acid group

    B : No treatment group

    Arm Description

    Patients in the Tranexamic Acid (TXA) group (arm-A) will be administered with 2 doses of intravenous tranexamic acid (cumulative dose 10ml=1g) as follows: the first dose 10 minutes before the surgical incision (1 vial of 5 ml = 0,5g by slow intravenous injection(=1ml/minute)), and the second 3 hours after the start of surgery (1 vial of 5 ml = 0,5g, by slow intravenous injection).

    In the control group, will not be administered TXA or any other drugs.

    Outcomes

    Primary Outcome Measures

    Postoperative anaemia
    Postoperative anaemia detected by daily measurements of haemoglobin in the first 3 days after surgery

    Secondary Outcome Measures

    Post-operative anaemia
    Post-operative anaemia reported as changes in haemoglobin and haematocrit values during the first 3 days after surgery.
    Intra-operative blood loss
    This outcome will be documented using a suction apparatus during the procedure. Blood collected in the suction bottle will be measured by subtracting the volume of saline used for wash.
    Post-operative blood loss at during the first 2 days after surgery
    This outcome will be documented using postoperative drain outputs. Blood collected in the drain outputs will be measured in milliliter at 24h and 48h
    Estimated total blood loss.
    This outcome will be documented using Hb balance formula.
    Estimated total blood loss.
    This outcome will be documented using Gross Formula.
    Blood transfusion requirements.
    This outcome will be documented in terms of number of patients who required packed red blood cell (PRBC) (transfusion rate) and the mean number of transfusion units per patient during all the length of hospitalization.
    Length of hospital stay
    Length of hospital stay
    Cost effectiveness of the treatment with tranexamic acid.
    This outcome will be documented reporting the mean cost per patient as sum of the cost TXA administration (if administered), the transfusion cost per patients, and the cost of hospital stay.

    Full Information

    First Posted
    March 10, 2021
    Last Updated
    October 5, 2021
    Sponsor
    Christian Candrian
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04803591
    Brief Title
    This is a Study to Verify if Tranexamic Acid Can Reduce the Anemia After a Femoral Shaft Fractures Surgery
    Acronym
    ORL-ORT-023
    Official Title
    Efficacy of Tranexamic Acid in Femoral Shaft Fractures Osteosynthesis; A Double Blind Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2021
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Not approved by Ethics Commettee
    Study Start Date
    August 1, 2021 (Anticipated)
    Primary Completion Date
    September 1, 2026 (Anticipated)
    Study Completion Date
    September 1, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Christian Candrian

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The investigators are going to evaluate if adding Tranexamic Acid in femoral shaft fractures surgery can lead to any advantages to the participants, namely if it can reduce post-operative anaemia, blood loss, blood transfusion requirements, length and cost of hospitalisation.
    Detailed Description
    Lower limb procedures represent the majority of orthopaedic surgeries, including joint arthroplasties, sport medicine treatments, and fractures osteo-synthesis, with a rate over 500 per 100,000 population every year, increasing. Albeit being successful procedures routinely performed in the clinical practice, they are frequently encumbered by complications. In particular, femur fractures are common and frequently result in considerable blood loss, ranging from 900 to 1,500 ml, which exposes patients to postoperative anaemia and reduced functional recovery. Allogenic blood transfusions are financial burden, and, even more, they are associated with an unneglectable risk of serious complications, including infection, immuno-suppression, cardiovascular dysfunction, resulting in potentially life-threatening effects on patients. Various strategies have been attempted to minimize blood loss and the need for blood transfusion, and to this aim the use of hemostatic agents, in particular of tranexamic acid (TXA), has recently widely increased in orthopaedic lower limb surgery. TXA is a synthetic anti-fibrinolytic agent that competitively blocks the lysine binding sites on plasminogen, thereby slowing the conversion of plasminogen to plasmin, thus preventing fibrin clot degradation. A large amount of randomized controlled trials and meta-analysis converge in showing that TXA, applied either through systemic or local administration, is effective in reducing blood loss and subsequent transfusions in lower limb fractures surgery, especially in hip fracture patients, as well in replacement procedures. However, there are still concerns about the risk of increasing venous thromboembolic (VTE) complications, such as deep venous thrombosis or pulmonary embolisms; overall, the scientific high-level literature evidence supports the safety of TXA for the different orthopaedic applications. This is a 2-arm study aimed at comparing the Tranexamic Acid supplementation protocol and evaluating his advantages over routine protocols. The primary objective will be the effect on postoperative anaemia, detected by serial measurements of haemoglobin, of TXA supplementation for femoral shaft fractures surgery. The secondary objectives of the study will be the comparison between I.V. peri-operative TXA supplementation and normal protocol without TXA in terms of post-operative anaemia (detected by serial haematocrit measurements), intra-operative blood loss, post-operative blood loss, total blood loss (evaluated using the Hb balance formula, estimated blood loss, blood transfusion requirements, length of hospitalisation, cost-effectiveness and frequency of adverse events. In particular the study aims to assess safety of TXA and its tolerability in terms of incidence of venous thromboembolic complications, such as deep venous thrombosis or pulmonary embolisms, wound infection, and death. The safety of TXA supplementation protocol will be verified comparing to the no-treatment group in terms of incidence of complications, such as deep venous thrombosis (based on the Homan sign and Mose sign and confirmed by compression ultrasonography upon clinical suspicion), Pulmonary embolism (confirmed by spiral computed tomography), cerebrovascular accident (confirmed by computed tomographic scan or magnetic resonance imaging), and acute coronary syndrome or myocardial infarction (confirmed by troponin I estimation and electrocardiogram changes), infection, and death. This randomized control trial will thus define if the peri-operative protocol should be implemented with tranexamic acid to reduce post-operative anaemia and blood loss and the rate of blood transfusion leading to a better cost effectiveness, without an increase in adverse events. The study presents only minimal risks for the included patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Femoral Shaft Fracture

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    A: Tranexamic Acid group
    Arm Type
    Experimental
    Arm Description
    Patients in the Tranexamic Acid (TXA) group (arm-A) will be administered with 2 doses of intravenous tranexamic acid (cumulative dose 10ml=1g) as follows: the first dose 10 minutes before the surgical incision (1 vial of 5 ml = 0,5g by slow intravenous injection(=1ml/minute)), and the second 3 hours after the start of surgery (1 vial of 5 ml = 0,5g, by slow intravenous injection).
    Arm Title
    B : No treatment group
    Arm Type
    No Intervention
    Arm Description
    In the control group, will not be administered TXA or any other drugs.
    Intervention Type
    Drug
    Intervention Name(s)
    Tranexamic Acid
    Other Intervention Name(s)
    TRANEXAM OrPha Inj Lös 500 mg/5ml
    Intervention Description
    Tranexamic Acid will be administered as an injectable solution (500mg/5ml or 1000mg/10ml).
    Primary Outcome Measure Information:
    Title
    Postoperative anaemia
    Description
    Postoperative anaemia detected by daily measurements of haemoglobin in the first 3 days after surgery
    Time Frame
    3 days after surgery
    Secondary Outcome Measure Information:
    Title
    Post-operative anaemia
    Description
    Post-operative anaemia reported as changes in haemoglobin and haematocrit values during the first 3 days after surgery.
    Time Frame
    3 days
    Title
    Intra-operative blood loss
    Description
    This outcome will be documented using a suction apparatus during the procedure. Blood collected in the suction bottle will be measured by subtracting the volume of saline used for wash.
    Time Frame
    Day 0
    Title
    Post-operative blood loss at during the first 2 days after surgery
    Description
    This outcome will be documented using postoperative drain outputs. Blood collected in the drain outputs will be measured in milliliter at 24h and 48h
    Time Frame
    Up to day 2
    Title
    Estimated total blood loss.
    Description
    This outcome will be documented using Hb balance formula.
    Time Frame
    Up to day 2
    Title
    Estimated total blood loss.
    Description
    This outcome will be documented using Gross Formula.
    Time Frame
    Up to day 2
    Title
    Blood transfusion requirements.
    Description
    This outcome will be documented in terms of number of patients who required packed red blood cell (PRBC) (transfusion rate) and the mean number of transfusion units per patient during all the length of hospitalization.
    Time Frame
    Up to day 2
    Title
    Length of hospital stay
    Description
    Length of hospital stay
    Time Frame
    Up to week 2
    Title
    Cost effectiveness of the treatment with tranexamic acid.
    Description
    This outcome will be documented reporting the mean cost per patient as sum of the cost TXA administration (if administered), the transfusion cost per patients, and the cost of hospital stay.
    Time Frame
    1 week

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Acute femoral shaft fracture. Patients treated surgically with intramedullary nail or femoral plate Patients aged 18-80 years old. Patients with a BMI >18.5 and <35. Patients able to provide informed consent and follow all the study procedures as indicated by the protocol. Informed Consent as documented by signature Exclusion Criteria: Pathological fracture or other lower limb fractures associated or multiple fractures. Use of any anticoagulant at the time of admission (eg, vitamin K antagonists, anti-thrombin agents, antiplatelet agents or factor IIa and Xa inhibitors). Contraindications to TXA (eg documented allergy to TXA). Hepatic dysfunction (aspartate transaminase (AST)/alanine transaminase (ALT)>60 U/l) or renal dysfunction (Cr >1.5 mg/dl of glomerular filtration rate (GFR)>30 ml/min). History of DVT or pulmonary embolus. Active coronary artery disease or cerebrovascular accident (event in the past 12 months). Coagulopathy based on admission laboratory values (international normalised ratio (INR)>1.4, partial thromboplastin time (PTT)>1.4× normal sec, platelets <50 000 per mm3) Women who are pregnant or breast feeding. Known or suspected non-compliance, drug or alcohol abuse. Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant. Participation in another study with investigational drug within the 30 days preceding and during the present study. Previous enrolment into the current study. Enrolment of the investigator, his/her family members, employees and other dependent persons.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Christian Candrian, MD; Prof.
    Organizational Affiliation
    EOC
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    URL
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    This is a Study to Verify if Tranexamic Acid Can Reduce the Anemia After a Femoral Shaft Fractures Surgery

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