In-hospital Cardiac Arrest - Dynamics and State Transitions

Sponsor
St. Olavs Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00920244
Collaborator
Norwegian Air Ambulance Foundation (Other), Norwegian University of Science and Technology (Other)
285
1
68
4.2

Study Details

Study Description

Brief Summary

The purpose of this study is to analyse transitions in cardiac rhythm and hemodynamic variables during resuscitation of patients with in-hospital cardiac arrest.

Condition or Disease Intervention/Treatment Phase

Detailed Description

In-hospital cardiac arrest carries a grave prognosis, with survival to discharge in the range of 15-20%. Key factors determining outcome include the presenting cardiac rhythm, aetiology, and early initiation of resuscitation. Some cardiac rhythms benefit from defibrillation (shockable rhythms). During resuscitation patients may switch between shockable and non-shockable rhythms, and may show signs of spontaneous circulation temporarily. Depending on rhythm and according to guidelines, patients receive direct current (DC) shocks (defibrillator) and/or i.v. adrenaline, atropine and amiodarone, which may affect state-transitions. We wish to make statistical analysis (time-series analysis, Markov modelling) of these state-transitions and variations in hemodynamic variables during resuscitation, related to CPR interventions and the cause of arrest. The cause of arrest will be determined based on chart records, interview with staff and autopsy if appropriate. One hypothesis is that differences in the patterns of state-transitions may reflect underlying aetiology, which may guide in future decision-making during resuscitation.

Study Design

Study Type:
Observational
Actual Enrollment :
285 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Dynamics and State Transitions During Resuscitation in In-hospital Cardiac Arrest
Study Start Date :
Aug 1, 2009
Actual Primary Completion Date :
Apr 1, 2015
Actual Study Completion Date :
Apr 1, 2015

Outcome Measures

Primary Outcome Measures

  1. Survival to discharge [1 year]

Secondary Outcome Measures

  1. Short-term survival [minutes-days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with in-hospital cardiac arrest who are resuscitated
Exclusion Criteria:
  • Younger than 18 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 St.Olavs Hospital, Department of Anesthesia Trondheim Norway 7014

Sponsors and Collaborators

  • St. Olavs Hospital
  • Norwegian Air Ambulance Foundation
  • Norwegian University of Science and Technology

Investigators

  • Study Chair: Eirik Skogvoll, MD, PhD, St. Olavs Hospital
  • Principal Investigator: Trond Nordseth, MD, St. Olavs Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
St. Olavs Hospital
ClinicalTrials.gov Identifier:
NCT00920244
Other Study ID Numbers:
  • 4.2008.2402 (REK)
  • 08/11457
  • 20708/2/IB
First Posted:
Jun 15, 2009
Last Update Posted:
Sep 5, 2018
Last Verified:
Aug 1, 2018

Study Results

No Results Posted as of Sep 5, 2018