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Neuroprotective Goal Directed Hemodynamic Optimization in Post-cardiac Arrest Patients (NEUROPROTECT)

Primary Purpose

Cerebral Ischemia, Cardiac Arrest

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Neuroprotective goal directed hemodynamic optimization
MAP > 65mmHg
Sponsored by
Universitaire Ziekenhuizen KU Leuven
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Ischemia focused on measuring post cardiac arrest, hemodynamics

Eligibility Criteria

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

Inclusion Criteria:

  1. Out-of-hospital CA of presumed cardiac cause irrespective of the presenting rhythm
  2. Unconsciousness (Glasgow coma scale < 8) at hospital admission
  3. Age ≥ 18 years
  4. Sustained return of spontaneous circulation (ROSC) (=when chest compressions have not been required for 20 consecutive minutes)

Exclusion Criteria:

  1. Suspected or confirmed intracranial bleeding or stroke
  2. Known limitations in therapy or Do Not Resuscitate-order
  3. Known disease compromising 180 day survival
  4. Known pre-CA cerebral performance category 3-4
  5. Previous stroke (TIA can be included)
  6. MRI incompatible cardiac or neurosurgical device
  7. Systolic blood pressure < 90 mmHg on norepinephrine > 1 mcg/kg/min).
  8. Open chest
  9. ECMO (extracorporeal membrane oxygenation)
  10. Pregnancy

Sites / Locations

  • Ziekenhuis Oost Limburg
  • UZ Leuven

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Neuroprotect

Control

Arm Description

MAP between 85-100mmHg SVO2 between 65-75%

MAP>65mmHg

Outcomes

Primary Outcome Measures

Diffusion weighted MRI
cerebral ischemia in post-cardiac arrest (CA) patients as quantified by the apparent diffusion coefficient (ADC) on diffusion weighted MRI (DW-MRI) to be performed at day 4- 5 post-CA using ADC scores in 11 pre-specified brain regions (frontal cortex, parietal cortex, temporal cortex, occipital cortex, precentral cortex, postcentral cortex, caudate nucleus, putamen, thalamus, cerebellum, pons).

Secondary Outcome Measures

diffusion weighted MRI
o Percentage of voxels under a suggested ADC threshold of 0.650x10-3 mm2/s
Diffusion weighted MRI
o Whole brain median ADC score [mm2/s]
CPC
o Cerebral performance category 3-5 at 180 days post-CA
The Short Form (36) Health Survey
o SF36 questionnaire at 180 days post-CA
Neurocognitive testing
Neurocognitive testing at discharge from the hospital by the adult verbal learning test
Neurocognitive testing
Neurocognitive testing at discharge from the hospital by the digit span backwards test
Neurocognitive testing
Neurocognitive testing at discharge from the hospital by the red pencil test
Neurocognitive testing
Neurocognitive testing at discharge from the hospital by the Wechsler Memory Scale Revised test
Biomarkers
Neuron specific enolase (day 1-2-3-4-5)
Functional testing
Activities Daily Life (ADL)
Functional testing
6 minute walking distance (6MWD) at discharge from the hospital
ICU parameters
lenght of stay in ICU [number of days]
ICU parameters
Ventilator days [number of days]
ICU parameters
tracheostomy performed (yes/no)
Renal function
creatinine [mg/dl]

Full Information

First Posted
August 27, 2015
Last Updated
June 21, 2018
Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
Ziekenhuis Oost-Limburg
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1. Study Identification

Unique Protocol Identification Number
NCT02541591
Brief Title
Neuroprotective Goal Directed Hemodynamic Optimization in Post-cardiac Arrest Patients
Acronym
NEUROPROTECT
Official Title
Neuroprotective Goal Directed Hemodynamic Optimization in Post-cardiac Arrest Patients: a Randomized Controlled Trial (the NEUROPROTECT Post-CA Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
August 2015 (undefined)
Primary Completion Date
June 2018 (Actual)
Study Completion Date
June 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
Ziekenhuis Oost-Limburg

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary objective of the Neuroprotect trial is to assess whether or not a new goal directed hemodynamic optimization strategy can reduce cerebral ischemia in post-cardiac arrest (CA) patients.
Detailed Description
Unconscious patients admitted to the intensive care unit after being successfully resuscitated from cardiac arrest (CA) are at high risk for death, and neurological deficits are common among survivors. Nevertheless, the optimal hemodynamic strategy to ensure optimal cerebral perfusion and maximal outcome has not been studied by a randomized controlled trial. In the absence of good evidence, current post-CA guidelines are adapted from sepsis guidelines and recommend targeting a mean arterial pressure (MAP) above 65 mmHg (Peberdy ea, Circulation 2010). Importantly, post-CA patients have a large cerebral penumbra at risk for infarction when resuscitated to suboptimal MAP's. In a large subset of post-CA patients the lower threshold of cerebral autoregulation is shifted rightward and these patients might benefit from resuscitation to higher MAP's (Sundgreen ea, Stroke 2001) in order to ensure adequate cerebral oxygenation. Our research group previously showed that a MAP of 85-100mmHg results in optimal cerebral perfusion in post-CA patients (Ameloot ea, resuscitation 2015). Two retrospective and 2 prospective observational studies suggested an association between higher MAP's and better outcome in post-CA patients (Ameloot ea, resuscitation 2015). However, the value of these trials is limited by their observational design. The question remains as to whether patients with higher MAP's do have a better outcome due to more optimal cerebral perfusion and less cerebral damage or whether a higher MAP is merely a non-causal marker of more limited disease severity in these patients. In other words, the primary research question is whether we can reduce cerebral ischemia and improve prognosis of post-cardiac arrest survivors by targeting higher mean systemic blood pressures thereby optimizing cerebral perfusion during their stay in the intensive care unit. To answer this, we propose a multicenter interventional open label investigator driven randomized controlled trial to compare a goal-directed potentially neuro-protective hemodynamic optimization strategy with the current standard of care. Primary efficacy endpoints of the study will include extent of cerebral damage as assessed with diffusion weighted magnetic resonance imaging (DW-MRI), functional and neurocognitive testing, biomarkers of brain injury and survival rates. The final utilization goal of the Neuroprotect post-CA trial is to show that our adapted hemodynamic protocol reduces cerebral ischemia, and improves survival and functional outcome of post-cardiac arrest patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Ischemia, Cardiac Arrest
Keywords
post cardiac arrest, hemodynamics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Neuroprotect
Arm Type
Experimental
Arm Description
MAP between 85-100mmHg SVO2 between 65-75%
Arm Title
Control
Arm Type
Active Comparator
Arm Description
MAP>65mmHg
Intervention Type
Other
Intervention Name(s)
Neuroprotective goal directed hemodynamic optimization
Intervention Type
Other
Intervention Name(s)
MAP > 65mmHg
Intervention Description
MAP > 65mmHg
Primary Outcome Measure Information:
Title
Diffusion weighted MRI
Description
cerebral ischemia in post-cardiac arrest (CA) patients as quantified by the apparent diffusion coefficient (ADC) on diffusion weighted MRI (DW-MRI) to be performed at day 4- 5 post-CA using ADC scores in 11 pre-specified brain regions (frontal cortex, parietal cortex, temporal cortex, occipital cortex, precentral cortex, postcentral cortex, caudate nucleus, putamen, thalamus, cerebellum, pons).
Time Frame
day 4-5
Secondary Outcome Measure Information:
Title
diffusion weighted MRI
Description
o Percentage of voxels under a suggested ADC threshold of 0.650x10-3 mm2/s
Time Frame
day 4-5
Title
Diffusion weighted MRI
Description
o Whole brain median ADC score [mm2/s]
Time Frame
day 4-5
Title
CPC
Description
o Cerebral performance category 3-5 at 180 days post-CA
Time Frame
180 days after admission
Title
The Short Form (36) Health Survey
Description
o SF36 questionnaire at 180 days post-CA
Time Frame
180 days after admission
Title
Neurocognitive testing
Description
Neurocognitive testing at discharge from the hospital by the adult verbal learning test
Time Frame
discharge from the hospital (expected time frame 2-4 weeks after admission)
Title
Neurocognitive testing
Description
Neurocognitive testing at discharge from the hospital by the digit span backwards test
Time Frame
discharge from the hospital (expected time frame 2-4 weeks after admission)
Title
Neurocognitive testing
Description
Neurocognitive testing at discharge from the hospital by the red pencil test
Time Frame
discharge from the hospital (expected time frame 2-4 weeks after admission)
Title
Neurocognitive testing
Description
Neurocognitive testing at discharge from the hospital by the Wechsler Memory Scale Revised test
Time Frame
discharge from the hospital (expected time frame 2-4 weeks after admission)
Title
Biomarkers
Description
Neuron specific enolase (day 1-2-3-4-5)
Time Frame
day 1-2-3-4-5
Title
Functional testing
Description
Activities Daily Life (ADL)
Time Frame
Discharge from the hospital (expected time frame 2-4 weeks after admission)
Title
Functional testing
Description
6 minute walking distance (6MWD) at discharge from the hospital
Time Frame
Discharge from the hospital (expected time frame 2-4 weeks after admission)
Title
ICU parameters
Description
lenght of stay in ICU [number of days]
Time Frame
At ICU discharge (expected time frame 1-2 weeks after admission)
Title
ICU parameters
Description
Ventilator days [number of days]
Time Frame
At ICU discharge (expected time frame 1-2 weeks after admission)
Title
ICU parameters
Description
tracheostomy performed (yes/no)
Time Frame
At ICU discharge (expected time frame 1-2 weeks after admission)
Title
Renal function
Description
creatinine [mg/dl]
Time Frame
day 1-2-3-4-5

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Out-of-hospital CA of presumed cardiac cause irrespective of the presenting rhythm Unconsciousness (Glasgow coma scale < 8) at hospital admission Age ≥ 18 years Sustained return of spontaneous circulation (ROSC) (=when chest compressions have not been required for 20 consecutive minutes) Exclusion Criteria: Suspected or confirmed intracranial bleeding or stroke Known limitations in therapy or Do Not Resuscitate-order Known disease compromising 180 day survival Known pre-CA cerebral performance category 3-4 Previous stroke (TIA can be included) MRI incompatible cardiac or neurosurgical device Systolic blood pressure < 90 mmHg on norepinephrine > 1 mcg/kg/min). Open chest ECMO (extracorporeal membrane oxygenation) Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Koen Ameloot, MD
Organizational Affiliation
UZ Leuven
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stefan Janssens, MD
Organizational Affiliation
UZ Leuven
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Joseph Dens, MD
Organizational Affiliation
Ziekenhuis Oost-Limburg
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Cathy De Deyne, MD
Organizational Affiliation
Ziekenhuis Oost-Limburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ziekenhuis Oost Limburg
City
Genk
ZIP/Postal Code
3600
Country
Belgium
Facility Name
UZ Leuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium

12. IPD Sharing Statement

Citations:
PubMed Identifier
33837117
Citation
Wouters A, Scheldeman L, Plessers S, Peeters R, Cappelle S, Demaerel P, Van Paesschen W, Ferdinande B, Dupont M, Dens J, Janssens S, Ameloot K, Lemmens R. Added Value of Quantitative Apparent Diffusion Coefficient Values for Neuroprognostication After Cardiac Arrest. Neurology. 2021 May 25;96(21):e2611-e2618. doi: 10.1212/WNL.0000000000011991. Epub 2021 Apr 9.
Results Reference
derived
PubMed Identifier
32792079
Citation
Ameloot K, Jakkula P, Hastbacka J, Reinikainen M, Pettila V, Loisa P, Tiainen M, Bendel S, Birkelund T, Belmans A, Palmers PJ, Bogaerts E, Lemmens R, De Deyne C, Ferdinande B, Dupont M, Janssens S, Dens J, Skrifvars MB. Optimum Blood Pressure in Patients With Shock After Acute Myocardial Infarction and Cardiac Arrest. J Am Coll Cardiol. 2020 Aug 18;76(7):812-824. doi: 10.1016/j.jacc.2020.06.043.
Results Reference
derived

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Neuroprotective Goal Directed Hemodynamic Optimization in Post-cardiac Arrest Patients

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