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ORthopaedic Trauma Anemia With Conservative Versus Liberal Transfusion (ORACL)

Primary Purpose

Anemia

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Blood and blood products for transfusion
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anemia

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Trauma patients admitted to participating hospital with any Orthopaedic injury who have been determined to be stable by the Trauma Service (General Surgery) and are no longer within the resuscitation phase of initial treatment. This is defined as a normal urine output (greater than 0.5 ml/kg/hr) and a systolic blood pressure greater than 90 mmHg for greater than 6 hours without fluid bolus or transfusion during that time
  • Age 18-50
  • Hemoglobin less than 9 g/dL or expected drop below 9 g/dL with planned surgery

Exclusion Criteria:

  • Pregnant ( urine pregnancy test will be done as standard of care)
  • Prisoner
  • Head injury (Glasgow Coma Scale less than 8 over 48 hours from presentation)
  • Known cardiac (coronary artery disease, atrial fibrillation, stent placement, congestive heart failure), renal (acute or chronic renal insufficiency or failure, defined as having Serum Creatinine >1.2 at time of enrollment), liver (Childs C cirrhosis) or pulmonary disease (chronic obstructive pulmonary disease, abnormal pulmonary function tests or history of poor pulmonary function from any cause including acute traumatic conditions such as ARDS)
  • Unlikely to follow up in the surgeon's estimation
  • Sickle Cell Anemia
  • History of cancer
  • Preexisting weakness, paresthesias, deformities, or other conditions which might affect functional outcome in the surgeon's opinion
  • Spinal cord injury
  • Patients with burns expected to require operative treatment
  • COVID positive

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Other

    Arm Label

    Liberal

    Conservative

    Arm Description

    Blood and blood products for transfusion. Transfusion will be done to keep Hgb >7 g/dL.

    Blood and blood products for transfusion. Transfusion will be done to keep Hgb > 5.5 g/dL.

    Outcomes

    Primary Outcome Measures

    Postoperative Wound Infection (Superficial or Deep) or Other Perioperative Infection
    Deep infection is defined as the need for intravenous antibiotics and/or a return to surgery for debridement. Superficial infection is defined as clinical diagnosis of cellulitis or other superficial infection treated with oral antibiotics only.

    Secondary Outcome Measures

    Combined Secondary Outcomes
    Combined (any) Secondary Outcomes: pulmonary embolism, deep venous thrombosis, acute renal failure or insufficiency, nonunion, delayed union, compartment syndrome, osteomyelitis, nerve palsy, anoxic brain injury, cardiac ischemia or infarct, pancreatitis, or death.
    Musculoskeletal Function Assessment
    The Musculoskeletal Function Assessment (MFA) evaluates the health status of patients with musculoskeletal disorders of the extremities, including patients with fractures and soft tissue injuries, repetitive motion disorders, osteoarthritis or rheumatoid arthritis. It describes patient functioning, assesses outcomes of surgical interventions and clinical trials, and monitors patients' functional status over time. The MFA is scored from 0 to 100 with 0 representing no dysfunction. Higher MFA scores/values represent a higher levels of dysfunction or worse outcome.

    Full Information

    First Posted
    November 17, 2016
    Last Updated
    June 28, 2023
    Sponsor
    Indiana University
    Collaborators
    Atlanta Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02972593
    Brief Title
    ORthopaedic Trauma Anemia With Conservative Versus Liberal Transfusion
    Acronym
    ORACL
    Official Title
    ORthopaedic Trauma Anemia With Conservative Versus Liberal Transfusion
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2014 (Actual)
    Primary Completion Date
    June 24, 2022 (Actual)
    Study Completion Date
    June 24, 2022 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Indiana University
    Collaborators
    Atlanta Medical Center

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The purpose of this study is to determine if there is a difference in outcomes between liberal transfusion (transfusing when hemoglobin drops below a set higher value number) and conservative transfusion (transfusing when hemoglobin drops below a set lower value number).
    Detailed Description
    Transfusion of Orthopaedic trauma patients is routinely done in asymptomatic individuals as there is no accepted national standard or recommendations from the American Academy of Orthopaedic Surgeons or the Orthopaedic Trauma Association for what level of anemia is appropriate in an asymptomatic patient. Individual practitioners typically make this decision based on anecdotal experiences and expert opinion. No prospective study has been performed to date to answer this question in this patient population. The null hypothesis of this proposed pilot study is that no difference will be seen with a liberal transfusion strategy to keep a patient's hemoglobin above 7 g/dL versus a conservative strategy to keep the patient's hemoglobin above 5.5 g/dL in patients asymptomatic at rest. The primary outcome of this pilot study will be infection; defined as postoperative wound infection (superficial or deep) or other perioperative infection but not surgical site (urinary tract infection or pneumonia). Deep infection is defined as the need for intravenous antibiotics or a return to surgery for debridement. Superficial infection is defined as the use of oral antibiotics only successfully treat a surgical site infection. Secondary outcomes will include pulmonary embolism, deep venous thrombosis, acute renal failure or insufficiency, nonunion, delayed union, compartment syndrome, osteomyelitis, nerve palsy, anoxic brain injury, cardiac ischemia or infarct, pancreatitis, or death, and the musculoskeletal functional assessment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Anemia

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    161 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Liberal
    Arm Type
    Other
    Arm Description
    Blood and blood products for transfusion. Transfusion will be done to keep Hgb >7 g/dL.
    Arm Title
    Conservative
    Arm Type
    Other
    Arm Description
    Blood and blood products for transfusion. Transfusion will be done to keep Hgb > 5.5 g/dL.
    Intervention Type
    Biological
    Intervention Name(s)
    Blood and blood products for transfusion
    Intervention Description
    Randomization would not occur until the patient's Hgb dropped below 7 g/dL. If the patient is randomized to the liberal arm, they would be transfused to keep their Hgb >7 g/dL. If the patient is randomized to the conservative arm, they would not be transfused until their Hgb drops below 5.5 g/dL. If the patient's Hgb does not drop below 7.0 g/dL, randomization will not be done.
    Primary Outcome Measure Information:
    Title
    Postoperative Wound Infection (Superficial or Deep) or Other Perioperative Infection
    Description
    Deep infection is defined as the need for intravenous antibiotics and/or a return to surgery for debridement. Superficial infection is defined as clinical diagnosis of cellulitis or other superficial infection treated with oral antibiotics only.
    Time Frame
    one year
    Secondary Outcome Measure Information:
    Title
    Combined Secondary Outcomes
    Description
    Combined (any) Secondary Outcomes: pulmonary embolism, deep venous thrombosis, acute renal failure or insufficiency, nonunion, delayed union, compartment syndrome, osteomyelitis, nerve palsy, anoxic brain injury, cardiac ischemia or infarct, pancreatitis, or death.
    Time Frame
    one year
    Title
    Musculoskeletal Function Assessment
    Description
    The Musculoskeletal Function Assessment (MFA) evaluates the health status of patients with musculoskeletal disorders of the extremities, including patients with fractures and soft tissue injuries, repetitive motion disorders, osteoarthritis or rheumatoid arthritis. It describes patient functioning, assesses outcomes of surgical interventions and clinical trials, and monitors patients' functional status over time. The MFA is scored from 0 to 100 with 0 representing no dysfunction. Higher MFA scores/values represent a higher levels of dysfunction or worse outcome.
    Time Frame
    one year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Trauma patients admitted to participating hospital with any Orthopaedic injury who have been determined to be stable by the Trauma Service (General Surgery) and are no longer within the resuscitation phase of initial treatment. This is defined as a normal urine output (greater than 0.5 ml/kg/hr) and a systolic blood pressure greater than 90 mmHg for greater than 6 hours without fluid bolus or transfusion during that time Age 18-50 Hemoglobin less than 9 g/dL or expected drop below 9 g/dL with planned surgery Exclusion Criteria: Pregnant ( urine pregnancy test will be done as standard of care) Prisoner Head injury (Glasgow Coma Scale less than 8 over 48 hours from presentation) Known cardiac (coronary artery disease, atrial fibrillation, stent placement, congestive heart failure), renal (acute or chronic renal insufficiency or failure, defined as having Serum Creatinine >1.2 at time of enrollment), liver (Childs C cirrhosis) or pulmonary disease (chronic obstructive pulmonary disease, abnormal pulmonary function tests or history of poor pulmonary function from any cause including acute traumatic conditions such as ARDS) Unlikely to follow up in the surgeon's estimation Sickle Cell Anemia History of cancer Preexisting weakness, paresthesias, deformities, or other conditions which might affect functional outcome in the surgeon's opinion Spinal cord injury Patients with burns expected to require operative treatment COVID positive
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Brian H Mullis, MD
    Organizational Affiliation
    Indiana University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    ORthopaedic Trauma Anemia With Conservative Versus Liberal Transfusion

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