Out of Hospital Cardiac Arrest: Trial Assessing the Survival Impact of Phone Advice

Summary

Medical call center have no phone advice protocol within out of hospital cardiac arrest in France. The purpose of the present study is to compare a group of patients with protocol phone advice delivered by the dispatchers ("CONTARM" group) versus usual phone advice ( "CONTHAB" group). Comparison will be performed on survival to seven days. The hypothesis is that CONTARM group has an higher survival at seven days. A second goal is to measure the survival to 15 and 30 days. The trial is randomized, controlled and will include 2600 patients. The patients will be enrolled in 19 hospitals in France.

Conditions

• Out of Hospital Cardiac Arrest

Interventions

OTHER

Protocol phone advice

Protocol phone advice

OTHER

Usual phone advice

Usual phone advice

Sponsors & Collaborators

• Centre Hospitalier Universitaire Dijon

  collaborator OTHER

• Central Hospital, Nancy, France

  collaborator OTHER

• University Hospital, Metz

  collaborator UNKNOWN

• University Hospital, Strasbourg, France

  collaborator OTHER

• Reims University hospital

  collaborator OTHER

• Centre Hospitalier de Lons Le Saunier

  collaborator UNKNOWN

• Groupe Hospitalier de la Region de Mulhouse et Sud Alsace

  collaborator OTHER

• Centre Hospitalier de Colmar

  collaborator OTHER

• Centre Hospitalier de Troyes

  collaborator OTHER

• Centre Hospitalier de Chalon sur Saône

  collaborator UNKNOWN

• Centre Hospitalier Universitaire de Nīmes

  collaborator OTHER

• Nantes University Hospital

  collaborator OTHER

• University Hospital, Bordeaux

  collaborator OTHER

• Hospices Civils de Lyon

  collaborator OTHER

• Poitiers University Hospital

  collaborator OTHER

• University Hospital, Angers

  collaborator OTHER_GOV

• University Hospital, Orléans

  collaborator UNKNOWN

• Centre Hospitalier de Montauban

  collaborator OTHER

• Centre Hospitalier Universitaire de Besancon

  lead OTHER

Study Design

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Model

PARALLEL

Eligibility

Min Age

18 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2016-10-12

Primary Completion

2021-10-12

Completion

2021-10-19

Countries

• France

Study Locations