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Impact of Speed Of Rewarming After CaRdiac Arrest and ThErapeutic Hypothermia (ISOCRATE)

Primary Purpose

Heart Arrest, Cardiac Arrest, Hypothermia

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Low Speed of Rewarming
High Speed of Rewarming
Sponsored by
Centre Hospitalier Departemental Vendee
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Arrest focused on measuring cardiac arrest, targeted temperature management, hypothermia induced, shockable rhythm

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient has been supported for a shockable cardiac arrest with successful resuscitation.
  • Coma persistent at ICU admission (Glasgow score less than or equal to 8) in the absence of sedation. If the patient is sedated in ICU admission, the glasgow score will be held the last evaluated by the doctor who provided the pre-hospital care of the patient score.
  • Body temperature> 33 ° C
  • Specific device used to targeted temperature management at 33°C

Exclusion Criteria:

  • Lack of witness of cardiac arrest.
  • Duration of no-flow> 10 minutes (time between the onset of cardiac arrest and the start of external cardiac massage).
  • Duration of low-flow> 60 minutes (the period between the start of external cardiac massage and recovery of an effective cardiac activity).
  • Major hemodynamic instability (dose norepinephrine and / or epinephrine > 1 µg / kg / min to maintain MAP> 65 mmHg).
  • Time between cardiac arrest and more than 480 minutes inclusion
  • Moribund.
  • Presence of histologically confirmed cirrhosis of Child class C.
  • Patient treatment in blocking the production of Il6 (Ro-tocilizumab or Actemra ®)
  • Patient under corticosteroid treatment (dose> 5 mg of prednisolone equivalent)
  • Pregnant woman, parturient or lactating.
  • Inpatient without consent and / or deprived of liberty by a court decision.
  • Patient under guardianship
  • Inclusion in advance a research protocol with the draw, and whose primary endpoint is on interleukin-6.
  • Lack of social security.
  • Refusal of the trusted person or patient.

Sites / Locations

  • Colin Gwenhael

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Low speed of rewarming

Fast speed of rewarming

Arm Description

Patients will be placed in targeted temperature controlled at 33°C for 24 hours. Then, intervention will be proceeded after randomization: slowly rewarmed (0.25°C/h) to targeted temperature controlled at 37°C for 24 hours.

Patients will be placed in targeted temperature controlled at 33°C for 24 hours. hen, intervention will be proceeded after randomization: fastly rewarmed (0.50°C/h) for targeted temperature controlled at 37°C for 24 hours.

Outcomes

Primary Outcome Measures

Interleukine 6 Dosage
Evolution of serum levels of Il6 (inflammation marker) measured 6 times between H0 (time of obtaining the thermal target) and H48

Secondary Outcome Measures

Neurological functional prognosis
Glasgow-Pittsburgh Cerebral Performance Category Score
Quality of Life-SF-36 score
36 items-Short Form for Health Survey telephonic interview
Life Autonomy
Modified Barthel, Index for activities of daily living (ADL) and two normative questions about life autonomy
Neurocognitive evaluation
Telephonic validated version of Mini mental state examination
Post traumatic stress disorders
Impact Event Scale-Revised
Mortality in the ICU
Mortality at hospital
Mortality at day 90
Duration of hospitalization in ICU
Duration of mechanical ventilation
Comparison of Interleukine 2
Comparison of Interleukine 4
Comparison of Interleukine 8
Comparison of Interleukine 10
Comparison of GM-CSF
Comparison of TNF-Alpha
Comparison of serum neurofilament
Comparison of CRP serum level
Comparison of procalcitonin serum level
Need for vasopressor treatment
vasopressor dose (Noradenaline or adrenalin)

Full Information

First Posted
September 14, 2015
Last Updated
March 11, 2022
Sponsor
Centre Hospitalier Departemental Vendee
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, University Hospital, Tours
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1. Study Identification

Unique Protocol Identification Number
NCT02555254
Brief Title
Impact of Speed Of Rewarming After CaRdiac Arrest and ThErapeutic Hypothermia
Acronym
ISOCRATE
Official Title
Impact of Speed Of Rewarming After CaRdiac Arrest and ThErapeutic Hypothermia. A Randomized Controlled Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
February 12, 2016 (Actual)
Primary Completion Date
May 17, 2020 (Actual)
Study Completion Date
June 8, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Departemental Vendee
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France, University Hospital, Tours

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Comparing the production of interleukin 6 (inflammatory cytokine) in two heating speed (slow rewarming rate: 0.25 ° C / h or fast rewarming rate 0.50 ° C / h) at the completion of a period of targeted temperature at 33°C after cardiac arrest supported by shockable rhythm and successfully resuscitated.
Detailed Description
Cardiac arrest (CA) is at present a major cause of mortality as well as a cause of disability for the surviving victims. In France, every year counts as 50,000 cardiac arrests responsible for 40 000 deaths. Thus, less than 20% of patients with heart failure discharged home. Then these patients had impaired quality of life associated with symptoms of fatigue, stress, anxiety hindering the resumption of business activity including. The prognosis is related in part to the initial cardiac rhythm present at the establishment of specialized resuscitation. Recent progress in improving mortality and neurological outcome has been achieved over the last decade with systematic implementation of a period of targeted temperature management between 32 and 34 ° C (TTM 32-34) in patients with cardiac arrest and who benefited from the completion of at least one external electrical shock when help arrived. The mechanisms underlying this improvement of neurological prognosis are many, but mainly related to an attenuation of post resuscitation syndrome that combines in one hand an inflammatory response (mediated by pro-inflammatory cytokines including interleukin 6) and secondly the formation of reperfusion injury related to the production of radical oxygen species (free radicals). While some studies have shown the feasibility of induction of this TTM 32-34 in prehospital conditions, no prospective study has evaluated the significant speed of warming in the end. An observational study in which the heating was carried passively, found that patients with an extended heating period (600 minutes) had a worse neurological outcome than patients with a duration of shorter warming (479 minutes) while a second retrospective study concluded the opposite in case of active warming . Besides the fact that these studies were observational, in the two originals randomized studies on TTM 32-34 in CA, the rate of warming was not like: Objective 6 hours with active warming is 0.5 ° C / h in the Australian study with an OR of 5.25 (1.47 - 18.76) for the neurological prognosis Objective 8 hours with passive warming of 0.37 ° C / h in the European study with an OR of 1.4 (1.08 - 1.81) for the neurological prognosis Although populations of two studies are obviously not comparable, it is possible that suboptimal speed of rewarming could mitigate some of the gain related to the implementation of TTM 32-34. In this context, investigators propose to conduct a randomized, single-center pilot study comparing a fast warming in a slow warming when performing a TTM 33 patients presented with a shockable cardiac arrest.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Arrest, Cardiac Arrest, Hypothermia
Keywords
cardiac arrest, targeted temperature management, hypothermia induced, shockable rhythm

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Low speed of rewarming
Arm Type
Experimental
Arm Description
Patients will be placed in targeted temperature controlled at 33°C for 24 hours. Then, intervention will be proceeded after randomization: slowly rewarmed (0.25°C/h) to targeted temperature controlled at 37°C for 24 hours.
Arm Title
Fast speed of rewarming
Arm Type
Experimental
Arm Description
Patients will be placed in targeted temperature controlled at 33°C for 24 hours. hen, intervention will be proceeded after randomization: fastly rewarmed (0.50°C/h) for targeted temperature controlled at 37°C for 24 hours.
Intervention Type
Procedure
Intervention Name(s)
Low Speed of Rewarming
Intervention Description
Speed of rewarming will be at 0.25°C/h with specific temperature controlled external device
Intervention Type
Procedure
Intervention Name(s)
High Speed of Rewarming
Intervention Description
Speed of rewarming will be at 0.50°C/h with specific temperature controlled external device
Primary Outcome Measure Information:
Title
Interleukine 6 Dosage
Description
Evolution of serum levels of Il6 (inflammation marker) measured 6 times between H0 (time of obtaining the thermal target) and H48
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Neurological functional prognosis
Description
Glasgow-Pittsburgh Cerebral Performance Category Score
Time Frame
Day 90
Title
Quality of Life-SF-36 score
Description
36 items-Short Form for Health Survey telephonic interview
Time Frame
Day 90
Title
Life Autonomy
Description
Modified Barthel, Index for activities of daily living (ADL) and two normative questions about life autonomy
Time Frame
Day 90
Title
Neurocognitive evaluation
Description
Telephonic validated version of Mini mental state examination
Time Frame
Day 90
Title
Post traumatic stress disorders
Description
Impact Event Scale-Revised
Time Frame
Day 90
Title
Mortality in the ICU
Time Frame
ICU Discharge (expected day 10)
Title
Mortality at hospital
Time Frame
Hospital Discharge (expected 20 days)
Title
Mortality at day 90
Time Frame
Day 90
Title
Duration of hospitalization in ICU
Time Frame
ICU Discharge (expected day 10)
Title
Duration of mechanical ventilation
Time Frame
Weaning of mechanical ventilation (expected day 7)
Title
Comparison of Interleukine 2
Time Frame
48 hours
Title
Comparison of Interleukine 4
Time Frame
48 hours
Title
Comparison of Interleukine 8
Time Frame
48 hours
Title
Comparison of Interleukine 10
Time Frame
48 hours
Title
Comparison of GM-CSF
Time Frame
48 hours
Title
Comparison of TNF-Alpha
Time Frame
48 hours
Title
Comparison of serum neurofilament
Time Frame
48 hours
Title
Comparison of CRP serum level
Time Frame
first seven days after admission
Title
Comparison of procalcitonin serum level
Time Frame
first seven days after admission
Title
Need for vasopressor treatment
Description
vasopressor dose (Noradenaline or adrenalin)
Time Frame
72 first hours after ICU admission

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient has been supported for a shockable cardiac arrest with successful resuscitation. Coma persistent at ICU admission (Glasgow score less than or equal to 8) in the absence of sedation. If the patient is sedated in ICU admission, the glasgow score will be held the last evaluated by the doctor who provided the pre-hospital care of the patient score. Body temperature> 33 ° C Specific device used to targeted temperature management at 33°C Exclusion Criteria: Lack of witness of cardiac arrest. Duration of no-flow> 10 minutes (time between the onset of cardiac arrest and the start of external cardiac massage). Duration of low-flow> 60 minutes (the period between the start of external cardiac massage and recovery of an effective cardiac activity). Major hemodynamic instability (dose norepinephrine and / or epinephrine > 1 µg / kg / min to maintain MAP> 65 mmHg). Time between cardiac arrest and more than 480 minutes inclusion Moribund. Presence of histologically confirmed cirrhosis of Child class C. Patient treatment in blocking the production of Il6 (Ro-tocilizumab or Actemra ®) Patient under corticosteroid treatment (dose> 5 mg of prednisolone equivalent) Pregnant woman, parturient or lactating. Inpatient without consent and / or deprived of liberty by a court decision. Patient under guardianship Inclusion in advance a research protocol with the draw, and whose primary endpoint is on interleukin-6. Lack of social security. Refusal of the trusted person or patient.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Baptiste Lascarrou, MD
Organizational Affiliation
Nantes University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Colin Gwenhael
City
La Roche Sur Yon
ZIP/Postal Code
85000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
34920723
Citation
Lascarrou JB, Guichard E, Reignier J, Le Gouge A, Pouplet C, Martin S, Lacherade JC, Colin G; AfterROSC network. Impact of rewarming rate on interleukin-6 levels in patients with shockable cardiac arrest receiving targeted temperature management at 33 degrees C: the ISOCRATE pilot randomized controlled trial. Crit Care. 2021 Dec 17;25(1):434. doi: 10.1186/s13054-021-03842-9.
Results Reference
derived

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Impact of Speed Of Rewarming After CaRdiac Arrest and ThErapeutic Hypothermia

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