An observational study in Cardiac Arrest, Out-Of-Hospital and Hypotension, sponsored by University of Massachusetts, Worcester. Recruiting at 8 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-27.
Sponsored by University of Massachusetts, Worcester · Observational
The goal of this study is to describe the population of patients presenting after out of hospital cardiac arrest with occult perfusion, defined as a patient without a palpable pulse but with some evidence of pulsatile arterial flow. The main questions it aims to answer are:
Researchers will describe the percentage of out-of-hospital cardiac arrest presenting to the emergency department without a pulse but with occult perfusion. Researchers will also compare survival endpoints (ROSC, Survival to hospital Admission, and Survival to Hospital Discharge) in pulseless patients with occult perfusion treated with ACLS interventions only and pulseless patients with occult perfusion treated as if they had pulsatile arterial flow.
Participants will undergo resuscitation based on decisions by the clinical team who incorporate echo and/or vascular ultrasound during the first three rounds of CPR. The resuscitation will continue until the patient demonstrates return of spontaneous circulation or until the clinical team halts resuscitative efforts due to futility.
This is a multi-center, prospective, observational trial involving sites across the United States and Canada. Patients having suffered an out of hospital cardiac arrest will be enrolled through the emergency department either presenting in cardiac arrest with ongoing CPR or having been resuscitated en-route but re-arresting shortly after arriving in the emergency department.
Patients will undergo any echocardiography or vascular ultrasound during the resuscitation at the discretion of the clinical team and based on institutional protocols. The clinical team will be unblinded to any aspect of the resuscitation, including the echo or vascular ultrasound images. Clinical interventions during the pause in CPR will be classified as ACLS interventions for cardiac arrest or non-ACLS interventions for occult perfusion. ACLS interventions include interventions for cardiac arrest such as bolus epinephrin or CPR. Non-ACLS interventions for occult perfusion include interventions for patients with profound hypotension such as continuous adrenergic agents or halting CPR to check a blood pressure.
Patients will be determined to have demonstrated occult perfusion based on blinded review of the patient data, ultrasound images, and vascular images.
Adjudicated Echo Image Review - Recorded cardiac images blinded to all patient and sonographer information will be reviewed by research staff to identify if a) cardiac activity is present and b) organized cardiac activity is present. Cardiac output will be measured as fractional shortening of the left ventricular chamber. Images will be reviewed separately by expert reviewers blinded to all patient information with adjudication by a third when there is disagreement.
Adjudicated Vascular Image Review - Recorded vascular images blinded to all patient and sonographer information will be reviewed by research staff to identify if arterial pulsations are visible. Measurements on the B-mode imaging will include a) artery diameter (superficial to deep) b) artery diameter (side to side) c) depth of artery from skin surface and d) area of the artery cross section at peak systole and peak diastole. The pulsatile index will be calculated as the ratio of the maximal artery diameter during a single pulsation (superficial to deep) to the minimal artery diameter during a single pulsation(superficial to deep). Images will be reviewed separately by expert reviewers blinded to all patient information with adjudication by a third when there is disagreement.
Patients will be classified as demonstrating occult perfusion with the following findings:
The study has a number of pre-determined study end points that are observational and associative in nature. They include the following:
314 studies on the registry are indexed under Out-of-Hospital Cardiac Arrest; 93 are open to participants now.
This study's planned enrollment of 1,400 is above the median of 300 across 128 observational studies indexed under Out-of-Hospital Cardiac Arrest.
Browse Out-of-Hospital Cardiac Arrest studies →University of Massachusetts, Worcester is the lead sponsor of 291 studies on the registry; 51 are open to participants now.
Of its 25 completed or terminated interventional studies of FDA-regulated products, 18 (72%) have results posted.
Counted across the registry records on this site, refreshed daily.
All patients presenting to the emergency department following atraumatic cardiac arrest with ongoing resuscitation will be considered for enrollment.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Patients presenting after cardiac arrest without a palpable pulse during pauses in CPR but echo or vascular ultrasound findings consistent with pulsatile arterial flow and treated as cardiac arrest with ACLS intervention such as rapid resumption of CPR, bolus epinephrine, or defibrillation.
Patients presenting after cardiac arrest without a palpable pulse during pauses in CPR but with echo or vascular ultrasound findings consistent with pulsatile arterial flow AND treated as hypotension with non-ACLS intervention such as continuous adrenergic agents, intravenous fluid, and extend pause in CPR to verify the presence of a measurable blood pressure.
Survival Rate (to Hospital Admission)
The percentage of patients that demonstrate survival that lasts long enough to be admitted to the hospital. Survival is defined as resumption of a sustained, perfusing cardiac activity after cardiac arrest characterized by restoring a palpable pulse, autonomous heart rhythm, and measurable blood pressure lasting long enough to be admitted to the hospital.
Time frame: Day 1
Return of Spontaneous Circulation
The percentage of patients that demonstrate a resumption of spontaneous coruscation (ROSC). ROSC is defined as the resumption of a sustained, perfusing cardiac activity after cardiac arrest characterized by restoring a palpable pulse, autonomous heart rhythm, and measurable blood pressure.
Time frame: Day 1
Survival to Hospital Discharge
The percentage of patients that demonstrate survival that lasts long enough to be discharged from the hospital.
Time frame: Up to 1 month
Plan to share: Yes — Only IPD used in the results publication will be shared
Supporting information: Study protocol, Clinical study report
Time frame: IPD sharing begins 12 months after article publication and will last for 5 years
Access criteria: Who will be able to access: Qualified researchers engaging in independent scientific research What they will be able to access: De-identified individual participant data sets, along with supporting documentation including the study protocol and the case report form. How they will be able to access it: Data is provided following the review and approval of a formal research proposal and statistical analysis plan, followed by the execution of a signed Data Sharing Agreement (DSA). Requests can be submitted via the contact email for the study PI.
No publications or documents are linked to this record.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
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