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Vasopressin and Epinephrine Versus Epinephrine Alone in Cardiac Arrest
This study has been completed.
First Received: August 5, 2005   Last Updated: October 16, 2007   History of Changes
Sponsor: Hospices Civils de Lyon
Information provided by: Hospices Civils de Lyon
ClinicalTrials.gov Identifier: NCT00127907
  Purpose

Recent studies have suggested that arginine-vasopressin could be more effective in the treatment of cardiac arrests. The last published study did not outline obvious improvements in the prognosis of all cardiac arrests but pointed out a possible increased survival rate when arginine-vasopressin is associated with epinephrine. The aim of this study is to compare the efficacy of two successive injections of epinephrine (1 mg) with two successive injections of epinephrine associated with arginine-vasopressin (40 UI) in out-of-hospital cardiac arrests occurring in adult patients. The primary endpoint is the survival rate at hospital admission. The inclusion period lasts 18 months and 2416 patients are planned to be enrolled.


Condition Intervention Phase
Cardiac Arrest
Drug: epinephrine (1 mg/1 mL)
Drug: arginine-vasopressin (40 UI/2 mL)
Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment
Official Title: Comparison of Epinephrine Associated With Vasopressin vs Epinephrine Alone in the Treatment of Out-of-Hospital Cardiac Arrests

Resource links provided by NLM:


Further study details as provided by Hospices Civils de Lyon:

Primary Outcome Measures:
  • Survival at hospital admission

Secondary Outcome Measures:
  • ROSC (Return of spontaneous circulation) Survival at : H24, Day 28, hospital discharge and one year Neurological status at H24 and hospital discharge.

Estimated Enrollment: 2416
Study Start Date: May 2004
  Eligibility

Ages Eligible for Study:   18 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Out-of-hospital medical cardiac arrest in adult patients.

Exclusion Criteria:

  • Traumatic cardiac arrest
  • Pregnancy
  • Patients younger than 18 years old or older than 85 years old
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00127907

Locations
France
Centre Hospitalier Lyon Sud
Pierre Bénite, France, 69495
Sponsors and Collaborators
Hospices Civils de Lyon
Investigators
Principal Investigator: Pierre-Yves GUEUGNIAUD, MD Hospices Civils de Lyon
  More Information

No publications provided by Hospices Civils de Lyon

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Study ID Numbers: 2003.329
Study First Received: August 5, 2005
Last Updated: October 16, 2007
ClinicalTrials.gov Identifier: NCT00127907     History of Changes
Health Authority: France: Afssaps - French Health Products Safety Agency

Keywords provided by Hospices Civils de Lyon:
Out-of-hospital cardiac arrest - Vasopressin - Epinephrine

Additional relevant MeSH terms:
Respiratory System Agents
Neurotransmitter Agents
Coagulants
Adrenergic Agents
Molecular Mechanisms of Pharmacological Action
Hematologic Agents
Physiological Effects of Drugs
Adrenergic Agonists
Arginine Vasopressin
Therapeutic Uses
Vasoconstrictor Agents
Vasopressins
Cardiovascular Diseases
Epinephrine
Heart Diseases
Adrenergic alpha-Agonists
Adrenergic beta-Agonists
Sympathomimetics
Anti-Asthmatic Agents
Heart Arrest
Cardiovascular Agents
Hemostatics
Pharmacologic Actions
Mydriatics
Natriuretic Agents
Autonomic Agents
Peripheral Nervous System Agents
Antidiuretic Agents
Bronchodilator Agents

ClinicalTrials.gov processed this record on November 25, 2009