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CAlcium and VAsopressin Following Injury Early Resuscitation (CAVALIER) Trial

Phase 2
Recruiting
Conditions
Trauma
Hemorrhage
Interventions
Registration Number
NCT05958342
Lead Sponsor
Jason Sperry
Brief Summary

The CAlcium and VAsopressin following Injury Early Resuscitation (CAVALIER) Trial is a proposed 4 year, double-blind, mutli-center, prehospital and early in hospital phase randomized trial designed to determine the efficacy and safety of prehospital calcium and early in hospital vasopressin in patients at risk of hemorrhagic shock.

Detailed Description

Resuscitation strategies for the acutely injured patient in hemorrhagic shock have evolved. Patients benefit from receiving less crystalloid in favor of blood transfusions with balanced ratios of plasma and platelets or whole blood resuscitation. These resuscitation practices are termed Damage Control Resuscitation and have been incorporated into resuscitation protocols in Level I trauma centers across the country. Damage Control Resuscitation represents standard practice for military and civilian trauma. Despite these changes, deaths from traumatic hemorrhage continue to occur in the first hours following trauma center arrival, underscoring the importance of early, novel interventions.

Hypocalcemia following traumatic injury is exceedingly common following severe traumatic injury in patients at risk of hemorrhagic shock. During hemorrhagic shock resuscitation, pathways reliant upon calcium such as platelet function, intrinsic and extrinsic hemostasis, and cardiac contractility are disrupted. Citrate containing transfusion products are known to further reduce calcium levels through chelation during trauma resuscitation. Hypocalcemia has consistently been shown to be independently associated with the risk of large volume blood transfusion and mortality. Current management practices include calcium replacement during the in hospital phase of care in patients receiving blood products. Early calcium replacement in patients at risk of hemorrhage and hypocalcemia may mitigate coagulopathy, maintain hemostasis, improve hemodynamics and outcomes, and may reduce complications attributable to hemorrhagic shock.

Arginine vasopressin is a physiologic hormone released by the posterior pituitary in response to hypotension and is commonly used as a vasopressor for critically ill patients for the treatment of hypotension due to multiple causes including sepsis. Prolonged hemorrhagic shock has the potential to alter systemic vasomotor tone which can progress to refractory/recalcitrant hypotension. Patients receiving resuscitation for hemorrhage are at risk of vasopressin deficiency. Vasopressin may improve hemostasis by enhancing platelet function and augmenting clot formation. Vasopressin infusion soon after injury in patients in hemorrhagic shock has been demonstrated to be safe and result in a reduction in blood transfusion requirements and a lower incidence of deep venous thrombosis.

Whole blood, red cells, and blood components are a precious and limited resource. Trauma resuscitation adjuncts such as early calcium and vasopressin may provide benefit when transfusion products are limited and may provide additional benefit even when transfusion capabilities remain robust. Due to their action on coagulation and hemodynamic cascades in the injured patient, these resuscitation adjuncts have the potential to interact and provide additive benefit to the injured patient. However, safety and efficacy of prehospital calcium and early in hospital vasopressin remain inadequately characterized. Enrolled patients may participate in the prehospital phase (calcium), in-hospital phase (vasopressin), or both. The aims of the CAlcium and VAsopressin following Injury Early Resuscitation (CAVALIER) trial are to determine the efficacy and safety of prehospital calcium supplementation and early in hospital vasopressin infusion as compared to standard care resuscitation in patients at risk of hemorrhagic shock and to appropriately characterize any additive effect of both resuscitation adjunct interventions.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1050
Inclusion Criteria

Prehospital Phase:

Injured patients at risk of hemorrhagic shock being transported from scene or referral hospital to a participating CAVALIER trial site who meet the following criteria:

1A. Systolic blood pressure ≤ 90mmHg and tachycardia (HR ≥ 108) at scene, at outside hospital, or during anticipated transport to a participating CAVALIER trial site

OR

1B. Systolic blood pressure ≤ 70mmHg at scene, at outside hospital, or during anticipated transport to a participating CAVALIER trial site

Early In-Hospital Phase:

Injured patients at a participating CAVALIER trial site at risk of hemorrhagic shock who meet the following criteria:

1A. Systolic blood pressure ≤ 90mmHg and tachycardia (HR ≥ 108) at scene, at outside hospital, during transport, or in emergency department of a participating CAVALIER trial site

OR

1B. Systolic blood pressure ≤ 70mmHg at scene, at outside hospital, during transport, or in emergency department of a participating CAVALIER trial site

AND

2.Blood/blood component transfusion initiated in prehospital setting or deemed clinically indicated within 60 minutes of arrival at the enrolling trauma center

AND 3. Clinical team deems Operating Room for major hemorrhage control procedure (e.g., laparotomy, thoracotomy, vascular exploration or extremity amputation) indicated within 60 minutes of arrival at the enrolling trauma center

AND

  1. Anticipated admission to intensive care unit (ICU)
Exclusion Criteria

Prehospital Phase

  1. Wearing NO CAVALIER opt-out bracelet
  2. Age > 90 or < 18 years of age
  3. Isolated fall from standing injury mechanism
  4. Known prisoner
  5. Known pregnancy
  6. Traumatic arrest with > 5 minutes of CPR without return of vital signs
  7. Brain matter exposed or penetrating brain injury
  8. Isolated drowning or hanging victims
  9. Objection to study voiced by subject or family member at the scene or at the trauma center
  10. Inability to obtain IV/IO access

Early In-Hospital Phase:

  1. Wearing NO CAVALIER opt-out bracelet
  2. Age > 90 or < 18 years of age
  3. Isolated fall from standing injury mechanism
  4. Known prisoner
  5. Known pregnancy
  6. Traumatic arrest with > 5 minutes of CPR without return of vital signs
  7. Brain matter exposed or penetrating brain injury
  8. Isolated drowning or hanging victims
  9. Objection to study voiced by subject or family member at the scene or at the trauma center
  10. Inability to obtain IV access

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Prehospital Intervention ArmCalcium Gluconate1 gram calcium gluconate provided via intravenous or intraosseous access over approximately 2-5 minutes, initiated prior to trauma bay arrival and infused to completion following arrival if needed
Prehospital Control Armsaline placeboIdentical volume saline placebo to prehospital intervention arm provided via intravenous or intraosseous access over approximately 2-5 minutes, initiated prior to trauma bay arrival and infused to completion following arrival if needed
Early In-Hospital Intervention ArmVasopressin4 unit vasopressin bolus followed by a vasopressin infusion at 0.04 U/min for eight hours, initiated within approximately two hours of enrollment
Early In-Hospital Control Armsaline placebovolume matched saline bolus followed by volume matched normal saline placebo infusion for eight hours initiated within approximately two hours of enrollment
Primary Outcome Measures
NameTimeMethod
Number of participants with 30-day mortalityfrom randomization to death or 30 days, whichever comes first

all cause mortality within 30 days

Secondary Outcome Measures
NameTimeMethod
Time to hemostasishospital arrival to 4 hours

Determined by ability to reach nadir transfusion requirement of 1 unit of red blood cells in a 60 minute period in the first 4 hours following arrival. In the absence of ability to obtain hemostasis within the first 4 hours, the patient will be designated "non-hemostasis"

Incidence of coagulopathy by thromboelastography (TEG)within 24 hours of arrival plus or minus 12

TEG date collected only when obtained as part of clinical

ICU free daysFrom hospital arrival to death or 30 days

number of days the patient is alive and not admitted to ICU subtracted from 30

Blood and blood component transfusion requirements in the initial 24 hoursfrom randomization to 24 hours

number of units transfused and type

Incidence of Multiple Organ Failure (MOF)Scores determined daily until up to Day 7 or ICU discharge, whichever comes first

Evaluated via the Denver Post injury Multiple Organ Failure Score, characterized as an incidence rate (percentage) and as MOF free days. Patients never admitted to ICU or with length of stay less than 48 hours will have a score of 0. A summary Denver score of \>3 will be classified as MOF.

Incidence of nosocomial infectionfrom randomization to death or 30 days

Utilizing the CDC criteria for diagnosis of hospital acquired pneumonia and blood stream infection

Number of participants with 6-hour mortalityfrom randomization to death or 6 hours, whichever comes first

all cause mortality within 6 hours

Number of participants with 24-hour mortalityfrom randomization to death or 24 hours, whichever comes first

all cause mortality within 24 hours

Number of participants with In-hospital mortalityIn hospital mortality from time of randomization to death or 30 days, whichever comes first

death prior to hospital discharge

Number of participants with Death from hemorrhagefrom randomization to death or 30 days, whichever comes first

Death from hemorrhage adjudicated by the site investigator

Number of participants with Death from brain injuryfrom randomization to death or 30 days, whichever comes first

Death from brain injury adjudicated by the site investigator

Blood and blood component transfusion requirements in the initial 6 hoursfrom randomization to 6 hours

number of units transfused and type

Hospital free daysFrom hospital arrival to death or 30 days

number of days the patient is alive and not admitted to hospital subtracted from 30

Ionized calcium measurementsMeasured in the first 60 minutes (+/- 3 hours), when feasible, during early stage resuscitation in emergency department or operating room

Ionized calcium collected as part of clinical care or as research lab

Trial Locations

Locations (2)

Allegheny Health Network

🇺🇸

Pittsburgh, Pennsylvania, United States

University of Pittsburgh

🇺🇸

Pittsburgh, Pennsylvania, United States

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