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NCT02344693 Clinical Trial

Electroencephalography in Patients Resuscitated From Cardiac Arrest

Cardiac Arrest Clinical Trial

Official title:
Electroencephalography in Patients Resuscitated From Cardiac Arrest

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02344693
Other study ID # 237/4 03.12.2012
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 1, 2017
Est. completion date December 2019

Study information
Verified date June 2018
Source Helsinki University Central Hospital
Contact Johannes Björkman, MD
Email johannes.bjorkman@helsinki.fi
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Sudden cardiac death can occur due to a multitude of causes. The underlying case can affect the overall prognosis. A return of spontaneous circulation not exceeding 30 minutes following a successful cardiopulmonary resuscitation is usually deemed imperative, if the patient is to survive. Monitors for evaluating the cardiac function during and after resuscitation are implemented on a daily basis (ekg, pulseoxymetry, blood pressure monitoring, cardiac sonography), but no devices for registration of the cortical brain activity exist. The aim of this study is to provide a 3-channel electroencephalogram using a prototype EEG/EKG adapter, connected to a Physio-Control LifePak 15 monitor/defibrillator, in patients who regain spontaneous circulation following non-traumatic cardiac arrest.

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Witnessed Cardiac Arrest

- Return of spontaneous circulation following cardiac arrest 10-40 min

Exclusion Criteria:

- traumatic cardiac arrest

- no consent from next-of-kin

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Finland Helsinki University Central Hospital Helsinki

Sponsors (1)
Lead Sponsor Collaborator
Helsinki University Central Hospital

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary prehospital EEG value in regard to patient discharge 60-min
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