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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01362556
Other study ID # BABICA
Secondary ID
Status Completed
Phase N/A
First received April 27, 2011
Last updated June 2, 2014
Start date March 2011
Est. completion date June 2014

Study information

Verified date June 2014
Source Medical University of Graz
Contact n/a
Is FDA regulated No
Health authority Austria: Agency for Health and Food Safety
Study type Interventional

Clinical Trial Summary

The debate over the administration of sodium bicarbonate in cardiac arrest has been going on for several decades, swinging like a pendulum from "first-line drug" to "not indicated" to the recent guidelines advocating "a small bolus under special conditions (metabolic acidosis, intoxication, long-term resuscitation)". A targeted, blood-gas controlled application under optimised ventilation conditions has not yet been evaluated prehospitally. Our preliminary studies have shown that an arterial puncture/line as well as measurement of blood gases is feasible in preclinical conditions. This multicentre trial including 5 centres and 10 physician-staffed emergency systems is designed to compare, in a prospective randomised controlled study, the effect of a calculated dosage of sodium bicarbonate based on the patient´s base deficit and weight, on ROSC (= return of spontaneous circulation) and on the secondary survival of cardiac arrest patients. The null hypothesis is that there is no or negative impact on survival.


Recruitment information / eligibility

Status Completed
Enrollment 700
Est. completion date June 2014
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- prehospitally started cardiopulmonary resuscitation (CPR)

- advanced cardiac life support provided

- age >18 years

- arterial pH < 7,2

- arterial BE < -12

- arterial pCO2 15-75 mmHg

- arterial pO2 >35 mmHg

Exclusion Criteria:

- women of childbearing age

- traumatic cardiac arrest

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Sodium bicarbonate
Administration of a calculated amount of sodium bicarbonate 8% [SB] after arterial blood gas measurement according to Base Excess [BE] and Body weight [kg]. Formula: SB [ml] = -BE * kg * 0.1
Sodium Chloride
Administration of a calculated amount of sodium chloride 0.9% [SC] after arterial blood gas measurement according to Base Excess [BE] and Body weight [kg]. Formula: SC [ml] = -BE * kg * 0.1

Locations

Country Name City State
Austria Landeskrankenhaus Bruck / Mur Bruck / Mur Styria
Austria LKH Graz West Graz Styria
Austria Medical University Graz Graz Styria
Austria Landeskrankenhaus Klagenfurt Klagenfurt Carinthia
Austria AKH Linz Linz Upper Austria
Austria Landesklinikum Wiener Neustadt Wiener Neustadt Lower Austria

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Graz

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of return of spontaneous circulation (ROSC) Within five hours from start of resuscitation. No
Secondary Survival to discharge after cardiac arrest Discharge from hospital participants will be followed for the duration of hospital stay, an expected average of 5 weeks No
Secondary Survival after one year of hospital discharge One year after event No
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