Effect of Xenon on Brain Injury After Aneurysmal Subarachnoid Hemorrhage

Cerebral Infarction Clinical Trial

— Xe-SAH  

Official title:

Effect of Xenon on Brain Injury, Neurological Outcome and Survival in Patients After Aneurysmal Subarachnoid Hemorrhage

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04696523
• Other study ID #: 109/2019 Xe-SAH
• Secondary ID: 2019-001542-17
• Status: Not yet recruiting
• Phase: Phase 2
• Start date: October 1, 2023
• Est. completion date: December 31, 2027

Study information

• Verified date: April 2023
• Source: Turku University Hospital
• Contact: Timo T Laitio, MD, PhD
• Phone: +358504653201
• Email: timo.laitio[@]tyks.fi
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

An investigator-initiated clinical drug study Main Objective: To explore neuroprotective properties of xenon in patients after aneurysmal subarachnoid hemorrhage (SAH). Primary endpoint: Global fractional anisotropy of white matter of diffusion tensor imaging (DTI). Hypothesis: White matter damage is less severe in xenon treated patients, i.e. global fractional anisotropy is significantly higher in the xenon group than in the control group as assessed with the 1st magnetic resonance imaging (MRI). After confirmation of aSAH and obtaining a signed assent subjects will be randomized to the following groups: Control group: Standard of Care (SOC) group: Air/oxygen and Normothermia 36.5-37.5°C; Xenon group: Normothermia 36.5-37.5°C +Xenon inhalation in air/oxygen for 24 hours. Brain magnetic resonance imaging techniques will be undertaken to evaluate the effects of the intervention on white and grey matter damage and neuronal loss. Neurological outcome will be evaluated at 3, 12 and 24 months after onset of aSAH symptoms Investigational drug/treatment, dose and mode of administration: 50±2 % end tidal concentration of inhaled xenon in oxygen/air. Comparative drug(s)/placebo/treatment, dose and mode of administration: Standard of care treatment according to local and international consensus reports. Duration of treatment: 24 hours Assessments: Baseline data Information that characterizes the participant's condition prior to initiation of experimental treatment is obtained as soon as is clinically reasonable. These include participant demographics, medical history, vital signs, oxygen saturation, and concentration of oxygen administered. Acute data The collected information will contain quantitative and qualitative data of aSAH patients, as recommended by recent recommendations of the working group on subject characteristics, and including all relevant Common Data Elements (CDE) can be applied. Specific definitions, measurements tools, and references regarding each SAH CDE can be found on the weblink here: https://www.commondataelements.ninds.nih.gov/SAH.aspx#tab=Data_Standards.

Description:

Assessments of efficacy: 1. A brain Computer tomography angiography (CTA) and / or 3 D Digital subtraction angiography (DSA) (whenever possible instead of 2D DSA) will be performed at hospital arrival and whenever clinically indicated. 2. 1st 3 Tesla MRI 72 ± 24 hours after onset of aSAH symptoms; 2nd 3 Tesla MRI 42 ± 4 days after onset of aSAH symptoms. 3. 3D DSA: Computational fluid dynamic simulations (CFD), artificial intelligence and machine learning. 4. Brain Positron emission tomography (PET): The 1st 4 ± 1 weeks and the 2nd at 3 months after onset of aSAH symptoms. 5. Biochemical assessment: A blood samples of 20 ml for determination of plasma catecholamines, plasma metabolomics (see details of metabolomics in section 18.4.7), cardiac enzyme release (P-hs-troponin-T and heart fatty-acid binding protein), selected biomarkers will be analysed at intensive crae unit (ICU) arrival and at 24h, at 48h and at 72h after onset of SAH symptoms. In addition, a sample of spinal fluid will be collected through external ventricular drainage (EVD) at ICU arrival or as soon as it is in place and at 24h, at 48h and at 72h after onset of SAH symptoms for assessment of metabolomics 6. Electrocardiograph (ECG) at ICU arrival and at 24h, at 48h and at 72h after onset of aSAH symptoms. 7. Neurological evaluation: at 3, 12 and at 24 months after aSAH with GOSe, Modified ranking score (mRS). Statistical methods: 1) Basic statistical tests (t-tests, Mann-Whitney, Chi square, etc); 2) Survival analysis methods; 3) An analysis of variance for repeated measurements; 4) A sample size of 100 is estimated on the basis of a recent studies in SAH patients to provide 80% power with a 2-sided α level of 0.05 to detect a mean difference of 0.02 (SD 0.035) in the global fractional anisotropy of white matter between the xenon group and the control group (98). Accordingly, this mean difference is estimated to have a predictive value for DCI and poor neurological outcome (i.e. mRS 3-6).Significance level of 0.05 and an estimation of 95 % confidence intervals will be used in the statistical analyses.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 160
• Est. completion date: December 31, 2027
• Est. primary completion date: December 31, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

To be considered eligible to participate in this study, a SAH subject must meet the

inclusion criteria listed below:

1. Informed consent obtained from the next of kin or legal representative

2. Aneurysmal subarachnoid hemorrhage visible on CTA or DSA.

3. Deterioration of consciousness to Hunt-Hess 3-5

4. Age of = 18 years

5. Intubated.

6. GCS 3-12 obtained off neuromuscular blocking agents

7. Xenon treatment can be started within 6 hours after onset of SAH symptoms Exclusion Criteria: An aSAH subject may not be enrolled in the trial if he/she meets any one of the exclusion

criteria below:

1. Acute or chronic traumatic brain injury

2. Maximum diameter of intracerebral hemorrhage > 2.5 cm

3. Pneumothorax or pneumomediastinum,

4. Acute lung injury requiring = 60% FIO2 (fraction of inspired oxygen).

5. Systolic arterial pressure < 80 mmHg or mean arterial pressure < 60 mmHg for over 30 min period

6. Bilaterally fixed and dilated pupils

7. Positive pregnancy test, known pregnancy, or current breast-feeding

8. Neurological deficiency due to traumatic brain injury or other neurological illness

9. Imminent death or current life-threatening disease

10. Current enrollment in another interventional study

11. The subject is known to have clinically significant laboratory abnormality, medical condition (such as decompensated liver disease or severe chronic obstructive pulmonary disease), or social circumstance that, in the investigator's opinion, makes it inappropriate for the subject to participate in this clinical trial.

12. Presence of implants or foreign bodies which are not known to be MRI safe

Related Conditions & MeSH terms

• Brain Injuries
• Brain Ischemia
• Cardiac Event
• Cardiac Failure
• Cerebral Infarction
• Cerebral Injury
• Cerebral Ischemia
• Heart Failure
• Hemorrhage
• Infarction
• Ischemia
• Subarachnoid Hemorrhage
• Subarachnoid Hemorrhage, Aneurysmal
• Wounds and Injuries

Intervention

Drug:
• Xenon
Xenon arm will be treated with xenon inhalation with endtidal concentration of 50 % in air/oxygen and with standard of care
• air/oxygen
Control group will be treated with air/oxygen

Locations

Country	Name	City	State
Finland	Aalto University School of Science	Helsinki
Finland	Kuopio University Hospital	Kuopio
Finland	Tampere University Hospital	Tampere
Finland	Elomatic	Turku
Finland	Turku University Hospital	Turku
Finland	University of Turku, Turku Bioscience, Analysis of the metabolomics	Turku
Sweden	Örebro University	Örebro

Sponsors (2)

Lead Sponsor	Collaborator
Turku University Hospital	Academy of Finland

Countries where clinical trial is conducted

Finland,  Sweden, 

References & Publications (2)

Arola O, Saraste A, Laitio R, Airaksinen J, Hynninen M, Backlund M, Ylikoski E, Wennervirta J, Pietila M, Roine RO, Harjola VP, Niiranen J, Korpi K, Varpula M, Scheinin H, Maze M, Vahlberg T, Laitio T; Xe-HYPOTHECA Study Group. Inhaled Xenon Attenuates My — View Citation

Laitio R, Hynninen M, Arola O, Virtanen S, Parkkola R, Saunavaara J, Roine RO, Gronlund J, Ylikoski E, Wennervirta J, Backlund M, Silvasti P, Nukarinen E, Tiainen M, Saraste A, Pietila M, Airaksinen J, Valanne L, Martola J, Silvennoinen H, Scheinin H, Har — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Fractional anisotropy of the white matter	Global fractional anisotropy of white matter of diffusion tensor imaging (DTI). Hypothesis: White matter damage is less severe in xenon treated patients, i.e. global fractional anisotropy is significantly higher in the xenon group than in the control group as assessed with the 1st MRI.	48-96 hours after start of aSAH symptoms
Secondary	Fractional anisotropy of white matter at cerebellum and/or at corpus callosum as assessed with the 1st MRI.	Fractional anisotropy of white matter at cerebellum and/or at corpus callosum as assessed with the 1st MRI.	48-96 hours after start of aSAH symptoms
Secondary	Safety and tolerability of xenon	Safety and tolerability of xenon as assessed with a ratio of adverse events, serious adverse events and suspected unexpected serious adverse reactions (SUSARs) during the follow-up of one year between the xenon group and the control group.	during the follow-up of one year
Secondary	Composite of radiological early brain injury (EBI) and delayed cerebral ischemia (DCI)	Composite of radiological EBI (within 72 hours after start of SAH symptoms) and DCI (Criterion of DCI: 1. a new focal neurological deficit (such as hemiparesis, aphasia, apraxia, hemianopia, or neglect) /decrease in level of consciousness (i.e. decrease of at least 2 points on the Glasgow Coma Scale; either on the total score or on one of its individual components, such as eye, motor on either side, or verbal). This should last for at least 1 hour and not is due to other causes (e.g. hydrocephalus, seizures, metabolic derangement, infection, sedation) and is not apparent immediately after aneurysm occlusion, and cannot be attributed to other causes by means of clinical assessment, CT or MRI scanning of the brain, and appropriate laboratory studies, 2. a new infarct on follow-up imaging (i.e. in any of the following: 2nd MRI, CT, CTA, DSA and perfusion CT) after 4 days post-SAH, or 3. both 1 and 2), and poor outcome at 3-months (good: mRS 0-2; poor: mRS 3-6) at 3-months and at 1 year	EBI: within first 72 hours after start of aSAH symptoms; mRS at 3 months and at 1 year and at 2 years after onset of aSAH symptoms
Secondary	Neurogenic Stress Cardiomyopathy and Stunned Myocardium	Neurogenic Stress Cardiomyopathy and Stunned Myocardium (i.e. myocardial injury caused by sympathetic storm and autonomic dysregulation with hs-troponin elevation, left ventricular dysfunction or ECG changes)	follow-up of 1 year
Secondary	Intracerebral pressure (ICP)	ICP level; Duration of therapy for ICP control/monitoring	during ICU stay up to 14 days after onset of aSAH symptoms
Secondary	Intracerebral pressure (ICP)	Need for ICP therapies (hypothermia, decompressive craniotomy)	during ICU stay up to 14 days after onset of aSAH symptoms
Secondary	Intracerebral pressure (ICP)	Duration of therapy for ICP control/monitoring	during ICU stay up to 14 days after onset of aSAH symptoms
Secondary	Plasma catecholamine level	Plasma level of noradrenaline , adrenaline, and dopamine	within 3 hours of ICU arrival, at 24h, 48h and 72 h after onset of aSAH symptoms
Secondary	Selected biomarkers	Selected biomarkers of brain injury: neurofilament light (NF-L), glial fibrillary acidic protein (GFAP), calcium binding protein S100B (S100B), ubiquitin carboxyterminal hydrolase L1 (UCH-L1), total tau, cytokines (tumour necrosis factor alpha, interleukins 6 and 10)	within 3 hours of ICU arrival and at 24h, at 48h and at 72h after onset of aSAH symptoms
Secondary	Development of prognostication models	Development of prognostication models with a selected combination of brain imaging, clinical data, biomarkers and metabolomics by applying artificial intelligence and machine learning for long-term outcome after aSAH	long-term outcome at 3 months, at 1 and at 2 years after onset of aSAH symptoms
Secondary	Development of prognostication models	Development of prognostication models with a selected combination of brain imaging, clinical data, biomarkers and metabolomics by applying artificial intelligence and machine learning for DCI after aSAH	between day 4 and 6 weeks after onset of aSAH symtoms
Secondary	Development of prognostication models	Development of prognostication models with a selected combination of brain imaging, clinical data, biomarkers and metabolomics by applying artificial intelligence and machine learning for vasospasm after aSAH	within 21 days after onset of aSAH symptoms
Secondary	Development of prognostication models	Development of prognostication models with a selected combination of brain imaging, clinical data, biomarkers and metabolomics by applying artificial intelligence and machine learning for EBI after aSAH	within 72 hours after onset of aSAH symtoms
Secondary	Difference of MRI parameters between xenon and control group	Difference of MRI parameters (fractional anisotropy, axial diffucivity, radial diffucivity of diffusion tensor imaging, DTI) between xenon and control group and in predicting risk for EBI	within 72 hours after onset of aSAH symptoms
Secondary	Difference of MRI parameters between xenon and control group	Difference of MRI parameters (fractional anisotropy, axial diffucivity, radial diffucivity of DTI) between xenon and control group and in predicting risk for vasospasm	within 21 days after onset of aSAH symptoms
Secondary	Difference of MRI parameters between xenon and control group	Difference of MRI parameters (fractional anisotropy, axial diffucivity, radial diffucivity of DTI) between xenon and control group and in predicting risk for DCI	between day 4 and 6 weeks after onset of aSAH symptoms
Secondary	Difference of MRI parameters between xenon and control group	Difference of MRI parameters (fractional anisotropy, axial diffucivity, radial diffucivity of DTI) between xenon and control group and in predicting risk for good/poor neurological outcome at 3 moths, at 1 year and at 2 years after onset of aSAH symptoms (mRS 0-2/mRS 3-6).	at 3 months, at 1 year and at 2 years after onset of aSAH symptoms
Secondary	Difference of CTA findings	Difference of CTA ischemic findings between xenon and control group and in predicting risk for EBI	within 72 hours after onset of aSAH symptoms
Secondary	Difference of CTA findings	Difference of ischemic findings in CTA between xenon and control group and in predicting risk for vasospasm	within 21 days after onset of aSAH symptoms
Secondary	Difference of CTA findings	Difference of ischemic findings in CTA between xenon and control group and in predicting risk for DCI	between day 4 and 6 weeks after onset of aSAH symptoms
Secondary	Difference of CTA findings between xenon and control group	Difference of ischemic findings in CTA between xenon and control group and in predicting risk for good/poor neurological outcome at 3 moths, at 1 year and at 2 years after onset of aSAH symptoms (mRS 0-2/mRS 3-6).	at 3 months, at 1 year and at 2 years after onset of aSAH symptoms
Secondary	Difference of DSA findings between xenon and control group	Difference of DSA findings indicating ischemic pattern of perfusion between xenon and control group and in predicting risk for EBI	within 72 hours after onset of aSAH symptoms
Secondary	Difference of DSA findings between xenon and control group	Difference of DSA findings indicating ischemic pattern of perfusion between xenon and control group and in predicting risk for vasospasm	within 21 days after onset of aSAH symptoms
Secondary	Difference of DSA findings between xenon and control group	Difference of DSA findings indicating ischemic pattern of perfusion between xenon and control group and in predicting risk for DCI	between day 4 and 6 weeks after onset of aSAH symptoms
Secondary	Difference of DSA findings between xenon and control group	Difference of DSA findings indicating ischemic pattern of perfusion between xenon and control group and in predicting risk for good/poor neurological outcome at 3 moths, at 1 year and at 2 years after onset of aSAH symptoms (mRS 0-2/mRS 3-6).	at 3 months, at 1 year and at 2 years after onset of aSAH symptoms
Secondary	Activity of microglia cells assessed with PET	It will be explored whether [11C](R)-PK11195 can be used to test the hypothesis of neuroprotective effect of xenon and to explore the role of inflammatory process for DCI after SAH. This could be demonstrated by showing less microglial activation in xenon group than in the reference therapy group and in the patients with good outcome, i.e. no DCI; Difference of activity of microglia cells between xenon and control group and in predicting risk for DCI	DCI between day 4 and 6 weeks after onset of aSAH symptoms; The 1st PETscan 4 ±1 weeks after onset of aSAH symptoms and the 2nd scan at 3 months after onset of SAH symptoms.
Secondary	Activity of microglia cells assessed with PET	It will be explored whether [11C](R)-PK11195 can be used to test the hypothesis of neuroprotective effect of xenon and to explore the role of inflammatory process for neurological outcome after SAH. This could be demonstrated by showing less microglial activation in xenon group than in the reference therapy group and in the patients with good outcome, i.e. mRS 0-2;	The 1st scan at 4 ±1 weeks after and the 2nd scan at 3 months after onset of SAH symptoms. Outcome: at 3 months, at 1 year and at 2 years after onset of aSAH symptoms
Secondary	Cerebral fluid dynamics	Predictive value of CFD simulations assessed with 3 dimensional DSA within 4 days of ICU arrival in predicting risk for EBI within 72 hours after onset of aSAH symptoms	Measures performed within 72 hours of ICU arrival
Secondary	Cerebral fluid dynamics	Predictive value of CFD simulations assessed with 3 dimensional DSA within 21 days of ICU arrival in predicting risk for neurological outcome at 3 months, at 1 year and at 2 years after SAH (mRS 0-2)	Measures performed within 21 days of ICU arrival; outcome at 3 months, at 1 year and at 2 years after onset of aSAH symptoms
Secondary	Cerebral fluid dynamics	Predictive value of CFD simulations assessed with 3 dimensional DSA within 21 days of ICU arrival in predicting risk for DCI within 6 weeks after onset of aSAH symptoms	Measures performed within 21 days of ICU arrival; DCI within 6 weeks after onset of aSAH symptoms