CAPACITY: Cognitive Auditory Evoked Potential After Cardiac Arrest: Interest of Mismatch negativiTY

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Completed
CT.gov ID
NCT01980446
Collaborator
(none)
85
2
1
66
42.5
0.6

Study Details

Study Description

Brief Summary

Determination of vital and functional outcome in comatose survivors after cardiac arrest is principally based on the identification of predictors of non-awakening, using by clinical, biological and electrophysiological tools. In patients without presence of non-awakening predictors, it would be of interest to identify predictive criteria of awakening. The presence of mismatch negativity during the cortical auditory-evoked potential could contribute to further progress in neurological prognostication of these patients. However, at this time, its prognostic value has been insufficiently studied and the optimal time of realization remains unknown.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Auditory-evoked potentials
N/A

Detailed Description

We hypothesized that the presence of the mismatch negativity during the cortical auditory-evoked potential would predict a favorable outcome in comatose survivors after cardiac arrest.The main objective is to determine the capacity of the presence of the mismatch negativity during the cortical auditory-evoked potential to predict a 1-year favorable outcome in comatose survivors after cardiac arrest

The secondary objectives are:
  • To assess the capacity of the presence of the mismatch negativity during the cortical auditory-evoked potential to predict awakening during the hospitalisation stay.

  • To determine the optimal time of realization of the cortical auditory-evoked potential

  • To determine the capacity of the presence of the mismatch negativity during the cortical auditory-evoked potential to predict ICU discharge and/or hospital discharge favorable outcome in comatose survivors after cardiac arrest

  • To determine the impact of the sedations drugs during the hypothermia phase, and during the ICU stay The main judgement criterion is the 1-year CPC score (CPC 1 to 2 as a favorable outcome)

Study design : Prospective, multicentre, interventional study. Decision making to withdrawal of life support will be strictly codified according current knowledge and standardized among the participating centres. In the absence of predictors of non-awakening, care will be continued without limitation. The design of the study will focus on the determination of the capacity of the presence of the mismatch negativity during the cortical auditory-evoked potential to predict awakening. Cortical auditory-evoked potential will be performed bedside in the ICU by qualified neurophysiologists. Results of cortical auditory-evoked potential will remain blinded of bedside clinicians providing care for the patients. Awakening will be assessed bedside daily. CPC score will be evaluated at discharge of the ICU, of the hospital, at 3 months and 1 year by an independent evaluator, blinded of the results of the cortical auditory-evoked potentials.

Study Design

Study Type:
Interventional
Actual Enrollment :
85 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Cognitive Auditory Evoked Potential After Cardiac Arrest: Interest of Mismatch negativiTY: The CAPACITY Study
Actual Study Start Date :
Dec 1, 2013
Actual Primary Completion Date :
Jun 1, 2018
Actual Study Completion Date :
Jun 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Other: 1:Mismatch negativity

Presence of the mismatch negativity during the cortical auditory-evoked potential would predict a favorable outcome in comatose survivors after cardiac arrest.

Procedure: Auditory-evoked potentials
cortical auditory-evoked potentials are performed to all included patients at inclusion, at day 5 to day 10, day without sedation (up to 1 year), day of awakening

Outcome Measures

Primary Outcome Measures

  1. CPC score of 1 or 2 (favorable outcome) [1 year]

    1-year CPC score of 1 or 2 (favorable outcome)

Secondary Outcome Measures

  1. Awakeness [up to 1 year]

    Awakeness during the hospitalisation stay

  2. Time of realization of the cortical auditory-evoked potential [up to 1 year]

    the optimal time of realization of the cortical auditory-evoked potential

  3. CPC score of 1 or 2 at ICU discharge [up to 1 year]

    the CPC score of 1 or 2 at ICU and at hospital discharge

  4. Length of mechanical ventilation, ICU stay, hospital stay and vital status at discharge [up to 1 year]

    impact of the sedations drugs during the ICU stay impact of therapeutic hypothermia

  5. CPC score of 1 or 2 at hospital discharge [up to 1 year]

    the CPC score of 1 or 2 at hospital discharge

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults (age ≥ 18 years)

  • hospitalized in the intensive care unit in the aftermath of a intra-or extra-hospital cardiac arrest

  • alive but remaining comatose between the 2nd day and the 5th day after cardiopulmonary arrest

Exclusion Criteria:
  • moribund patients (treatment limitations or the life expectancy of the inclusion estimated at less than 1 year)

  • patient awake at day of potential inclusion

  • brain death state

  • failure to realize the cortical

  • patient whose hearing loss is known

Contacts and Locations

Locations

Site City State Country Postal Code
1 Lariboisière Hospital - Medical and toxicology unit Paris France 75010
2 Dr Stéphane LEGRIEL - Intensive Care Unit Versailles France 78150

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris

Investigators

  • Principal Investigator: Stephane LEGRIEL, MD, Versailles Hospital - 78150 Le Chesnay - France

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT01980446
Other Study ID Numbers:
  • P091118
  • 2010-A01378-31
First Posted:
Nov 11, 2013
Last Update Posted:
Aug 20, 2020
Last Verified:
Aug 1, 2020
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 20, 2020