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EEG in Resuscitated In-hospital Patients

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ClinicalTrials.gov Identifier: NCT02349087
Recruitment Status : Recruiting
First Posted : January 28, 2015
Last Update Posted : October 31, 2018
Sponsor:
Information provided by (Responsible Party):
Kuopio University Hospital

Tracking Information
First Submitted Date January 23, 2015
First Posted Date January 28, 2015
Last Update Posted Date October 31, 2018
Study Start Date December 2014
Estimated Primary Completion Date December 2018   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: January 23, 2015)
24 hours of EEG monitoring starting from resuscitation and quantity of non-convulsive status epilepticus found [ Time Frame: 24 hours ]
Original Primary Outcome Measures Same as current
Change History Complete list of historical versions of study NCT02349087 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title EEG in Resuscitated In-hospital Patients
Official Title Integrating EEG Into Acute Medicine: EEG in Resuscitated In-hospital Patients
Brief Summary In Kuopio University Hospital Department of Clinical Neurophysiology there have been designed a fast EEG electrode, that is suitable for acute emergency use. This study will address the clinical use of acute EEG with this fast EEG electrode in in- hospital patients who have been resuscitated due to cardiac arest. After resuscitation patients will be treated in ICU and EEG will be recorded for 24 hours.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Probability Sample
Study Population In- hospital resuscitated patients, who are going to be treated in ICU after ROSC. Patients with Do Not Attempt to Resuscitate -decision will not be included.
Condition
  • Sudden Cardiac Arrest
  • Seizures
Intervention Device: Acute EEG with fast applicable EEG electrode
Study Groups/Cohorts Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Recruiting
Estimated Enrollment
 (submitted: January 23, 2015)
50
Original Estimated Enrollment Same as current
Estimated Study Completion Date December 31, 2018
Estimated Primary Completion Date December 2018   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Resuscitated in-hospital patients

Exclusion Criteria:

  • Patients with Do Not Attempt to Resuscitate-decision
  • Patients who are not going to be treated in ICU after resuscitation
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts
Contact: Stepani Bendel, MD, PhD 358 44 7175539 stepani.bendel@kuh.fi
Contact: Sanna Savikkomaa, MD 358 44 7175039 sanna.savikkomaa@kuh.fi
Listed Location Countries Finland
Removed Location Countries  
 
Administrative Information
NCT Number NCT02349087
Other Study ID Numbers KUH507T010
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Kuopio University Hospital
Study Sponsor Kuopio University Hospital
Collaborators Not Provided
Investigators
Study Director: Esa Mervaala, MD, PhD,prof Clinical Neurophysiology
PRS Account Kuopio University Hospital
Verification Date October 2018