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TerminatedNCT03477006PPOWERUpdated Oct 6, 2021Results posted

Pragmatic Prehospital Group O Whole Blood Early Resuscitation Trial

A Phase 3 interventional study of Whole blood in Hemorrhagic Shock, sponsored by Jason Sperry. Terminated at 1 site in United States. Open to participants aged 18 Years to 89 Years. Per ClinicalTrials.gov, last updated 2021-10-06.

Sponsored by Jason Sperry · Phase 3, Interventional, and Treatment

Why this study was terminated
Slow enrollment, financial considerations and global pandemic
Phase
Phase 3
Study type
Interventional
Enrollment
86
Allocation
Randomized
Ages
18 Years to 89 Years
Sex
All
01

Study summary

Despite advances in trauma resuscitation, a paucity of therapeutic interventions are available early enough to reduce the downstream morbidity and mortality attributable to hemorrhage, shock and coagulopathy. Due to the time sensitive nature of the treatment of hemorrhage, the ideal resuscitation intervention would entail use of a blood product containing all essential hemostatic components, closest to time of injury, where prevention or reversal of the devastating downstream consequences of shock and coagulopathy can occur. This proposal will characterized the efficacy of whole blood resuscitation initiated in the prehospital setting to patients in hemorrhagic shock which represents this ideal intervention post-injury. These results will have great potential to dramatically change the way trauma resuscitation occurs today.

Read the detailed description

Traumatic injury represents an incredible health care burden in the United States and worldwide. Hemorrhage is estimated to be responsible for over 40% of all trauma-related deaths. Ongoing traumatic blood loss is complicated by the well-known 'lethal triad' of coagulopathy, hypothermia and acidosis which results in further unbridled hemorrhage. Uncontrolled bleeding, resultant shock and organ dysfunction remain the leading causes of early in-hospital mortality. Despite advances in trauma resuscitation, a paucity of therapeutic interventions are available early enough to reduce the downstream morbidity and mortality attributable to hemorrhage, shock and coagulopathy.

In-hospital resuscitation of traumatic hemorrhage has changed over the past decade. The underlying principle of current resuscitation practice focuses on preventing or reversing the effects of coagulopathy with the early use of a balanced component transfusion strategy (1:1:1 - plasma: packed red blood cells: platelets). This reconstituted strategy has also been coined 'whole blood-like' resuscitation despite being inferior compositionally to whole blood. The use of whole blood was historically the gold standard for treating hemorrhagic shock during World War I and II, prior to sweeping changes in blood banking practice. Whole blood use continues today and is thought to provide the bleeding patient the identical components they are losing with maximal resuscitative and hemostatic effects.

Recent military experiences continue to show the benefits of fresh whole blood resuscitation demonstrating significant survival and hemostatic advantages. Whole blood has also been postulated to improve microcirculatory hemodynamics, reduce the 'storage lesion' effect and minimize donor exposure risks. A recent civilian study has also demonstrated benefit using modified whole blood after arrival to the hospital where appropriate blood typing and cross matching was performed prior to transfusion. Due to the time sensitive nature of the treatment of hemorrhage, the ideal resuscitation intervention would entail use of a blood product containing all essential hemostatic components, closest to time of injury, where prevention or reversal of the devastating downstream consequences of shock and coagulopathy can occur.

Initiation of whole blood resuscitation in the prehospital setting and continued through the in-hospital phase of treatment to patients in hemorrhagic shock represents this ideal intervention post-injury. Essential to the prehospital initiation of whole blood resuscitation in the civilian population is need for it to be transfused without the need for blood typing or cross matching. Of similar importance is the need for cold storage and recycling of any unused whole blood product, allowing maximal utility of this precious resource.

Based upon the belief that early whole blood resuscitation represents the most efficacious hemostatic resuscitation product for the management of hemorrhage, the University of Pittsburgh is currently utilizing cold stored, low titer, platelet replete-leukocyte reduced, group O whole blood (LTLR-WB) for urgent release in the emergency department, without the need for blood typing or cross matching, for patients in hemorrhagic shock. The hypothesis is that the initiation of LTLR-WB resuscitation in the prehospital setting with continuation through the in-hospital acute resuscitation phase of care will significantly reduce the morbidity and mortality attributable to hemorrhagic shock post-injury as compared to standard prehospital and in-hospital resuscitation practice. Thus, a large pragmatic clinical trial is needed to definitively establish the efficacy and safety of whole blood resuscitation initiated in the prehospital setting. Only a high quality clinical trial will provide the essential evidence to justify and provide the impetus for the use of this precious blood banking resource early post-injury. Because of the challenges associated with execution of these types of large trials particularly in the prehospital setting, it is essential to establish feasibility of this approach in a pilot study and provide experience to inform a definitive large, multicenter whole blood trial. The University of Pittsburgh has a track record of prehospital interventional trials post-injury and the clinical research infrastructure to successfully execute the following this trial.

02

Conditions studied

  • Hemorrhagic Shock

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03

Who can participate

Ages eligible
18 Years to 89 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Injured patients being transport via an air medical service with hypotension (SBP =/\< 90mmHg with tachycardia >108 OR SBP=/\<70 without the tachycardia requirement)

Exclusion criteria

Exclusion Criteria:

Age \< 18 or > 89 years

Isolated fall from standing injury mechanism

Brain matter exposed or penetrating brain injury (GSW)

CPR > 5 mins with out ROSC

Isolated burns without evidence of traumatic injury

Isolated Drowning or Hanging

No Intravenous or Intraosseous access

Known prisoner or known pregnancy

Referral Hospital Admission

Wearing No PPOWER bracelet

Objection to study voiced by subject or family at scene

04

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
86 participants (actual)

Study arms

  • Experimental
    LTLR-WB

    Receiving 2 units of low titer, leucocyte reduced, platelet replete whole blood initiated in the prehospital setting during air medical transport and continued (up to 6 units of whole blood followed by standard component resuscitation) thru the early in-hospital phase of care

    Biological: Whole blood

  • No intervention
    Standard Care

    Receiving standard prehospital air medical care and standard of care component (1:1:1) trauma resuscitation thru the early in-hospital phase of care

Interventions

  • BiologicalWhole blood

    Low titer, group O, leukocyte reduced, platelet replete, cold stored whole blood

05

What researchers measure

Primary outcomes

  1. 28 Day All Cause Mortality

    28 day all cause mortality

    Time frame: 28 days from admission

Secondary outcomes

  1. Incidence of Multiple Organ Failure

    multiple organ failure using the Denver post-injury MOF score which is a summed score and when the score is 4 or greater from 4 organ system scores, MOF is designated; 4 organ systems (pulmonary \[0-3\], renal \[0-3\], hepatic \[0-3\], cardiovascular \[0-3\])

    Time frame: 28 days from admission

  2. 24 Hour Mortality

    24 hour mortality

    Time frame: 24 hours from admission

06

Results

Posted Oct 6, 2021

Participant flow

Participant flow — Overall Study
MilestoneLTLR-WBStandard Care
Started4046
Completed4046
Not completed00

Outcome measures

Primary28 Day All Cause Mortality

28 day all cause mortality

Time frame:
28 days from admission
Reported as:
Count of participants · Participants
28 Day All Cause Mortality
ParticipantsLTLR-WBStandard Care
28 Day All Cause Mortality1012
Statistical analysis
  • LTLR-WB vs Standard Care · Chi-squared · p = 0.91
SecondaryIncidence of Multiple Organ Failure

multiple organ failure using the Denver post-injury MOF score which is a summed score and when the score is 4 or greater from 4 organ system scores, MOF is designated; 4 organ systems (pulmonary \[0-3\], renal \[0-3\], hepatic \[0-3\], cardiovascular \[0-3\])

Time frame:
28 days from admission
Reported as:
Count of participants · Participants
Incidence of Multiple Organ Failure
ParticipantsLTLR-WBStandard Care
Incidence of Multiple Organ Failure49
Statistical analysis
  • LTLR-WB vs Standard Care · Chi-squared · p = 0.23
Secondary24 Hour Mortality

24 hour mortality

Time frame:
24 hours from admission
Reported as:
Count of participants · Participants
24 Hour Mortality
ParticipantsLTLR-WBStandard Care
24 Hour Mortality68
Statistical analysis
  • LTLR-WB vs Standard Care · Chi-squared · p = 0.76

Adverse events

Collected over During Hospital admission up to 28 days. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
LTLR-WB10/40 (25%)7/40 (17.5%)0/40 (0%)
Standard Care12/46 (26.1%)11/46 (23.9%)1/46 (2.2%)
Most frequent serious events
Most frequent serious events
EventLTLR-WBStandard Care
ARDSRespiratory, thoracic and mediastinal disorders3/401/46
strokeNervous system disorders1/403/46
DVTBlood and lymphatic system disorders1/403/46
RhabdomyolysisMusculoskeletal and connective tissue disorders1/402/46
pulmonary embolusRespiratory, thoracic and mediastinal disorders1/401/46
gastrointestinal bleedGastrointestinal disorders0/401/46
Most frequent other events
Most frequent other events
EventLTLR-WBStandard Care
hyponatremiaMetabolism and nutrition disorders0/401/46

Baseline characteristics

Age, Continuous
Age, Continuous(years)LTLR-WBStandard CareTotal
Median46 (27 to 64)51 (36 to 62)48.5 (33 to 62)
Sex: Female, Male
Sex: Female, Male(Participants)LTLR-WBStandard CareTotal
Female233154
Male171532
Race (NIH/OMB)
Race (NIH/OMB)(Participants)LTLR-WBStandard CareTotal
American Indian or Alaska Native000
Asian000
Native Hawaiian or Other Pacific Islander000
Black or African American426
White344377
More than one race000
Unknown or Not Reported213
Region of Enrollment
Region of Enrollment(participants)LTLR-WBStandard CareTotal
United States404686
07

Study locations

1 site
  • University of Pittsburgh
    Pittsburgh, Pennsylvania 15213, United States
08

References and documents

Publications

  • Guyette FX, Zenati M, Triulzi DJ, Yazer MH, Skroczky H, Early BJ, Adams PW, Brown JB, Alarcon L, Neal MD, Forsythe RM, Zuckerbraun BS, Peitzman AB, Billiar TR, Sperry JL. Prehospital low titer group O whole blood is feasible and safe: Results of a prospective randomized pilot trial. J Trauma Acute Care Surg. 2022 May 1;92(5):839-847. doi: 10.1097/TA.0000000000003551. Epub 2022 Jan 25. PubMed 35081595 ↗

Study documents

  • Protocol and statistical analysis plan · Feb 4, 2020

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Registry details

Key details

Study ID
NCT03477006
Lead sponsor
Jason Sperry
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Responsible party
Jason Sperry (Professor of Surgery and Critical Care Medicine, University of Pittsburgh) — Sponsor-investigator
First posted
Mar 26, 2018
Start date
Nov 20, 2018
Primary completion
Oct 30, 2020
Completion
Oct 30, 2020
Results posted
Oct 6, 2021
Last update
Oct 6, 2021

Study contacts

Jason Sperry, MD
principal investigator · University of Pittsburgh

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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