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aICP Measurement in Patients With Cerebral Artery Infarction / aICP MCA Infarction (aICPStroke)

Primary Purpose

Stroke, Acute

Status
Suspended
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Vittamed 205 Non-invasive intracranial pressure (ICP) meter
Sponsored by
Kantonsspital Aarau
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Stroke, Acute

Eligibility Criteria

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

Inclusion Criteria:

  • Patient with an ischemic stroke in the internal carotid artery or middle cerebral artery territory at risk of a malignant MCA evolution, defined based on clinical presentation, clinical course (showing a progressive deterioration of conscious within the first 24-48 h), and neuroradiological findings.
  • Age: ≥ 18 years at admission
  • Informed consent of the patient or consent of patient's next of kin (plus consent of an independent physician)

Exclusion Criteria:

  • Patients with wounds, scars including the front orbital region.
  • Patients with any known ocular condition that may be worsened by sustained eye pressure.

Sites / Locations

  • Kantonsspital Aarau AG

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Stroke patients with ICP measurement

Arm Description

All patients with the possibility to evolve a malignant MCA infarct according to the initial assessment, will be included in our study, to measure ICP non-invasive. The ICP will be measured non-invasive with the Vittamed 205 Non-invasive intracranial pressure (ICP) meter.

Outcomes

Primary Outcome Measures

Increased intracranial pressure
The primary outcome is the non-invasive, absolute intra-cranial pressure (ICP) in M-MCA patients before decompressive surgery, as determined by the "non-invasive ICP absolute value meter" in mmHg

Secondary Outcome Measures

Correlation of ICP, neuroimaging and transcranial color Doppler
Correlation between non-invasive measured ICP and clinical and neuroimaging findings and standard transcranial color Doppler

Full Information

First Posted
August 7, 2018
Last Updated
February 25, 2020
Sponsor
Kantonsspital Aarau
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1. Study Identification

Unique Protocol Identification Number
NCT03641963
Brief Title
aICP Measurement in Patients With Cerebral Artery Infarction / aICP MCA Infarction
Acronym
aICPStroke
Official Title
Non-invasive Absolute Intracranial Pressure Measurement in Patients With Malignant Middle Cerebral Artery Infarction for Determination of Timing to Decompressive Craniectomy
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Suspended
Why Stopped
Safety questions on patients with glaucoma are in discussion by our IRB
Study Start Date
December 1, 2018 (Actual)
Primary Completion Date
September 30, 2019 (Actual)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kantonsspital Aarau

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Space-occupying, malignant middle cerebral artery (M-MCA) infarctions are still one of the most devastating forms of ischemic stroke, with a mortality of up to 80% in untreated patients. It is reported that early hemicraniectomy leads to a substantial decrease in mortality at 6 and 12 months and is likely to improve functional outcome. Thus, this study investigates if non-invasive intracranial pressure (ICP) measuring could represent an objective value to determine the time point to indicate decompressive craniectomy surgery. However, there are still important questions about the individual indication for decompressive surgery. In consideration of a variable clinical course (some patients develop fatal brain edema early, whereas other patients do not show severe brain swelling for several days), achieving a way to measure, control and predict malignant brain edema formation would be of extremely important value.
Detailed Description
Space-occupying, malignant middle cerebral artery (M-MCA) infarctions are still one of the most devastating forms of ischemic stroke, with a mortality of up to 80% in untreated patients. Actually, M-MCA infarctions constitute between 1% to 10% of all supratentorial ischemic strokes, with a yearly incidence about 10-20/100.000 people. The etiology of malignant MCA infarctions is mostly due to thrombosis or embolic occlusion of either the internal carotid artery or the proximal MCA. The term M-MCA is referred to a severe MCA syndrome with typical clinical symptoms (hemiparesis to hemiplegia, severe sensory deficits, head and eye deviation, hemi-inattention, and, if the dominant hemisphere is involved, global aphasia), following a uniform clinical course (progressive deterioration of conscious within the first 24-48 h), and ending in herniation. An early diagnosis is essential and depends on CT (Computed Tomography) and MRI (Magnetic Resonance Imaging) to aid the prediction of a malignant course, but, until today there is no clear consensus to define and predict radiologically a malignant evolution in early phases. Several pharmacological strategies have been proposed but the efficacy of these approaches has not been supported by adequate evidence from clinical trials and, until recently, treatment of malignant MCA infarctions has been a major unmet need. Over the past 10 years, results from randomised controlled trials (RCT) (HAMLET, DECIMAL and DESTINY) and their pooled analyses have provided evidence that an early hemicraniectomy leads to a substantial decrease in mortality at 6 and 12 months and is likely to improve functional outcome. However, there are still important questions about the individual indication for decompressive surgery. In consideration of a variable clinical course (some patients develop fatal brain edema early, whereas other patients do not show severe brain swelling for several days), achieving a way to measure, control and predict malignant brain edema formation would be of extremely important value. In this way, the ICP measuring could represent an objective value to determine in every patient the time point to indicate decompressive craniectomy surgery, and also could allow us to find a correlation between the size of the infarction and periinfarction edema. Therefore the optimal timing of surgical intervention can be defined and all the medical treatment adjusted. Currently, ICP can be measured and registered only using invasive techniques. The two ICP measurement methods available - intraventricular and intraparenchymal - require both a neurosurgical procedure, in order to implant the catheter and probes within the brain. Thus, these measures include themselves a risk for the subject, and both infections and intracranial bleedings are regular albeit not frequent complications. In addition, invasive recording of ICP requires neurosurgical expertise and intensive care unit (ICU) facilities. Therefore ICP measurement so far, is not a standard of care in stroke units. A reliable, accurate and precise non-invasive method to measure ICP would be of considerable clinical value, enabling ICP measurement without neurosurgical expertise and ICU facilities. Moreover, it would save the patients from the complication risks associated with invasive measures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Acute

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Stroke patients with ICP measurement
Arm Type
Experimental
Arm Description
All patients with the possibility to evolve a malignant MCA infarct according to the initial assessment, will be included in our study, to measure ICP non-invasive. The ICP will be measured non-invasive with the Vittamed 205 Non-invasive intracranial pressure (ICP) meter.
Intervention Type
Device
Intervention Name(s)
Vittamed 205 Non-invasive intracranial pressure (ICP) meter
Intervention Description
Non-Invasive intracranial pressure measurement
Primary Outcome Measure Information:
Title
Increased intracranial pressure
Description
The primary outcome is the non-invasive, absolute intra-cranial pressure (ICP) in M-MCA patients before decompressive surgery, as determined by the "non-invasive ICP absolute value meter" in mmHg
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Correlation of ICP, neuroimaging and transcranial color Doppler
Description
Correlation between non-invasive measured ICP and clinical and neuroimaging findings and standard transcranial color Doppler
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient with an ischemic stroke in the internal carotid artery or middle cerebral artery territory at risk of a malignant MCA evolution, defined based on clinical presentation, clinical course (showing a progressive deterioration of conscious within the first 24-48 h), and neuroradiological findings. Age: ≥ 18 years at admission Informed consent of the patient or consent of patient's next of kin (plus consent of an independent physician) Exclusion Criteria: Patients with wounds, scars including the front orbital region. Patients with any known ocular condition that may be worsened by sustained eye pressure.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Javier Fandino
Organizational Affiliation
Kantonsspital Aarau
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital Aarau AG
City
Aarau
ZIP/Postal Code
5001
Country
Switzerland

12. IPD Sharing Statement

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aICP Measurement in Patients With Cerebral Artery Infarction / aICP MCA Infarction

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