NCT04876222

Brief Summary

In patients with Out-of-Hospital Cardiac arrest who achieves Return Of Spontaneous Circulation (ROSC) The investigators want to evaluate whether there is a benefit from acute Angiography compared to subacute (12-24 hours) Angiography

Trial Health

60
Monitor

Trial Health Score

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

Enrollment
212

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started May 2021

Longer than P75 for not_applicable

Geographic Reach
2 countries

7 active sites

Status
terminated

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

First Submitted

Initial submission to the registry

April 30, 2021

Completed
3 days until next milestone

Study Start

First participant enrolled

May 3, 2021

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 6, 2021

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 22, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 22, 2026

Completed
Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

5 years

First QC Date

April 30, 2021

Last Update Submit

April 22, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Major Adverse Cardiovascular Events

    Mortality, cardiogenic shock or recurrent cardiac arrest

    30-day

Secondary Outcomes (24)

  • Mortality

    30-day and 1-year and 5-year

  • Cardiogenic shock

    30-day and 1-year

  • Recurrent cardiac arrest

    30-day and 5-year

  • Revascularization

    30-day and 1-year

  • Cerebral Performance Category score

    30-day and 6-month

  • +19 more secondary outcomes

Study Arms (2)

Acute CAG

ACTIVE COMPARATOR

The patient is triaged directly to the catheterization laboratory for acute evaluation including ECHO, acute CAG and PCI if indicated according to guidelines.

Procedure: Acute CAG

Subacute CAG

NO INTERVENTION

The patient is triaged to the coronary care unit (CCU) for rhythm surveillance, and additional diagnostics, and in case there is found indication for CAG, it is planned for the coming day in daytime (12-24 hours after cardiac arrest). Revascularization is performed if indicated according to guidelines.

Interventions

Acute CAGPROCEDURE

The patient is triaged directly to the catheterization laboratory for acute evaluation including ECHO, acute CAG and PCI if indicated according to guidelines.

Acute CAG

Eligibility Criteria

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

You may qualify if:

  • Witnessed Cardiac Arrest
  • ROSC
  • CAG possible within 120 minutes
  • Glasgow coma scale \>8

You may not qualify if:

  • Age \< 18 years
  • Obvious non-cardiac cause for the arrest
  • Terminal illness
  • STEMI

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (7)

Aalborg University Hospital

Aalborg, Denmark, Denmark

Location

Rigshospitalet

Copenhagen, Denmark, Denmark

Location

Odense University Hospital

Odense, Denmark, 5000, Denmark

Location

Christian Juhl Terkelsen

Aarhus, 8200, Denmark

Location

Department of cardiology, Aarhus University Hospital in Skejby

Aarhus, 8200, Denmark

Location

Catharina Zeikenhuis

Eindhoven, 5623, Netherlands

Location

Radboud Universitair Medisch Centrum

Nijmegen, 6525, Netherlands

Location

MeSH Terms

Conditions

Out-of-Hospital Cardiac ArrestComa

Condition Hierarchy (Ancestors)

Heart ArrestHeart DiseasesCardiovascular DiseasesUnconsciousnessConsciousness DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

April 30, 2021

First Posted

May 6, 2021

Study Start

May 3, 2021

Primary Completion

April 22, 2026

Study Completion

April 22, 2026

Last Updated

April 28, 2026

Record last verified: 2026-04

Locations