NCT07002294

Brief Summary

This randomized clinical trial will determine if adult participants who are in the emergency department after being resuscitated from a cardiac arrest outside of the hospital benefit from care delivered at specialized centers. The main question that it will answer is whether transferring participants to a hospital with a specialized cardiac arrest service improves recovery of function after 90 days. Participants will receive all usual medical care, but some participants will be offered transfer to a regional cardiac arrest center and others will be offered care at the closest appropriate hospital. Investigators will interview participants after 90 days to assess their recovery.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,618

participants targeted

Target at P75+ for not_applicable

Timeline
68mo left

Started Jun 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress1%
Jun 2026Jan 2032

First Submitted

Initial submission to the registry

May 23, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 3, 2025

Completed
12 months until next milestone

Study Start

First participant enrolled

June 1, 2026

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2031

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2032

Last Updated

February 5, 2026

Status Verified

July 1, 2025

Enrollment Period

5 years

First QC Date

May 23, 2025

Last Update Submit

February 3, 2026

Conditions

Keywords

cardiac arrest

Outcome Measures

Primary Outcomes (1)

  • Modified Rankin Scale

    The Modified Rankin Scale (mRS) is a measure of functional recovery, measured 90 days after cardiac arrest. A Modified Rankin Score (mRS) of 0 corresponds to full functional recovery and a Modified Rankin Score (mRS) of 6 corresponds to death, with progressively worse functional outcomes at higher scores. Intermediate values reflect progressive functional dependence, with higher scores reflecting greater dependence on others.

    90 Days post arrest

Secondary Outcomes (3)

  • Survival to ICU Admission

    24 hours post arrest

  • 72 hour survival

    72 hours post arrest

  • mRS at hospital discharge

    Up to 6 months post arrest

Study Arms (2)

Transfer to specialty care

EXPERIMENTAL

Participants randomized to receive specialty care will undergo immediate interfacility transport to and hospital treatment at the specialty care hospital

Other: Transfer to specialty care

Usual care

ACTIVE COMPARATOR

Participants randomized to the usual care arm will be hospitalized at the first hospital or transferred to the closest appropriate hospital

Other: Usual care

Interventions

Interfacility transport and treatment at the specialty care hospital

Transfer to specialty care

Hospitalization and treatment at the closest appropriate facility

Usual care

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Out-of-hospital cardiac arrest
  • Resuscitated from cardiac arrest with palpable pulse in the emergency department
  • Treated at one of participating hospital emergency departments
  • Age ≥18 years

You may not qualify if:

  • Known prior advanced directives or decision to limit critical care
  • Known pre-arrest dependent functional status (e.g., living in a skilled nursing facility, hospice or bedbound)
  • Arrest in the emergency department \>4 hours after arrival
  • Traumatic etiology of arrest
  • Known to have opted-out from the SPARC trial

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Pittsburgh Department of Emergency Medicine

Pittsburgh, Pennsylvania, 15213, United States

Location

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Related Links

MeSH Terms

Conditions

Heart ArrestOut-of-Hospital Cardiac Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Jonathan Elmer, MD, MS

    University of Pittsburgh

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Sara DiFiore-Sprouse

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

May 23, 2025

First Posted

June 3, 2025

Study Start

June 1, 2026

Primary Completion (Estimated)

June 1, 2031

Study Completion (Estimated)

January 1, 2032

Last Updated

February 5, 2026

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will share

Deidentified data may be shared in the future with investigators at other institutions. The local investigators will execute data use agreements with outside investigators and institutions prior to sharing any data. Identifiable data will not be shared.

Locations