Surviving PEA in Roanoke (SPEAR) Study
The Carilion Clinic and Virginia Tech Carilion School of Medicine, in conjunction with Roanoke Fire-EMS, Botetourt County Department of Fire \& EMS and Salem Fire-EMS, are studying the outcomes of patients experiencing Pulseless Electrical Activity (PEA). PEA refers to a type of cardiac arrest in which there is normal electrical activity in the heart however the heart still fails to contract to generate a pulse. Without heart contractions, which normally generates a pulse, the brain and other important organs fail to receive blood and oxygen. Unfortunately, the majority (97.3%) of patients that experience this rhythm do not survive and most don't even make it to the hospital. This study is trying to determine if the administration of a High Calcium, Low Sodium (HCLS) fluid in pre-hospital care will improve the chances of survival. Generally, a sodium (salt) solution is provided to patients experiencing cardiac arrest. Studies have shown that lower sodium and higher calcium content may activate certain parts of the heart cells required to generate a pulse under PEA conditions. This study is a double-blind, prospective, clinical trial. PEA patients will randomly receive either routine fluid therapy (salt solution) or a HCLS solution. While HCLS solution is not the standard fluid used by EMS providers responding to PEA, it is composed of FDA approved components and is occasionally used by EMS providers at their discretion in treating PEA. It is predicted that HCLS will either improve PEA survival or deliver similar outcomes as routine treatment. All patients will receive standard, high quality cardiac arrest and post-cardiac arrest care regardless of assigned treatment group.
Conditions:
🦠 Cardiac Arrest 🦠 Pulseless Electrical Activity
🗓️ Study Start (Actual) 16 February 2022
🗓️ Primary Completion (Estimated) February 2027
✅ Study Completion (Estimated) February 2027
👥 Enrollment (Estimated) 342
🔬 Study Type INTERVENTIONAL
📊 Phase PHASE2
Locations:
📍 Roanoke, Virginia, United States

📋 Eligibility Criteria

Description

    Inclusion Criteria:

    • * All patients who present with PEA at any time during the patients' treatment by Roanoke Fire-EMS, Botetourt County Department of Fire \& EMS and/or Salem Fire-EMS. This study defines a PEA presentation as any patient who is unconscious, presenting without a carotid pulse and with non-(VT/VF) ventricular tachycardia/ventricular fibrillation electrical activity.

    Exclusion Criteria:

    • * Patient less than 18 years old
    • * Known pregnancy
    • * Duration of untreated cardiac arrest of more than 30 minutes
    • * Traumatic cardiac arrest
    • * Known (LVAD) Left Ventricular Assist Device
    • * Rapidly fatal underlying disease
    • * Known or suspected digitalis toxicity
    • * A physical, durable (DNR) Do Not Resuscitate (or durable DNR medical jewelry) presented to EMS before treatment with asserting a preference not to be enrolled
    • * Prisoners and other populations with involuntary consent
Ages Eligible for Study: 18 Years to N/A (ADULT, OLDER_ADULT)
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No

🗓️ Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

  • First Submitted 20 February 2022
  • First Submitted that Met QC Criteria 8 March 2022
  • First Posted 17 March 2022

Study Record Updates

  • Last Update Submitted that Met QC Criteria 8 March 2022
  • Last Update Posted 17 March 2022
  • Last Verified March 2022