Chronic Kidney DiseaseNCT03342183
Reducing Hemodialysis Induced Recurrent Brain Injury to Improve Patients' Lives
A study testing Intervention Arm in people with Chronic Kidney Disease, run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's at 1 site in Canada.
Trial summary
Patients who receive dialysis for kidney failure suffer severe cognitive impairment. Hemodialysis causes circulatory stress and ischemia, which causes severe brain injury. It has been demonstrated that a procedure known as Remote Ischemic Preconditioning(RIPC), which involves wrapping a blood pressure cuff around a… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Kidney Disease
- What is being tested?
- Intervention Arm
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 25 participants
- Where
- 1 siteCanada
- Study dates
- 8 Jan 2018to 12 Oct 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male or Female
- Having hemodialysis treatment at least three times per week
- Must be 18 years old or older.
- Ability to speak and understand English
Who cannot join
- Exposure to hemodialysis for less than 90 days prior to recruitment
- Established severe cognitive impairment (Montreal Cognitive Assessment test (MoCA) of less than 18 or with a formal diagnosis of dementia)
- Previous clinical stroke
- Taking drugs to blunt response to RIPC (e.g. ciclosporin, ATP-sensitive potassium channel directed drugs)
- Dialysing using lower limb vascular access
- Pregnancy, breastfeeding, or intending pregnancy
- Unable to give consent or understand written information
Trial locations and contacts
1 site in 1 country.
About this study
Patients who receive dialysis for kidney failure suffer severe cognitive impairment. Hemodialysis causes circulatory stress and ischemia, which causes severe brain injury. It has been demonstrated that a procedure known as Remote Ischemic Preconditioning(RIPC), which involves wrapping a blood pressure cuff around a patient's leg and inflating has the potential of protecting many organs, such as the heart from the effects of dialysis. Our study aims to investigate this phenomenon to determine the extent to which it provides protection to a dialysis patient's brain.
Read the detailed description
Hemodialysis patients suffer severe cognitive impairment: Abnormalities of cognitive impairment (predominately sub-cortical defects in executive decision making) are almost universal in hemodialysis (HD) patients and appear early after starting dialysis. Around 75% of patients exhibit mild cognitive impairment (MCI) and a high proportion (˜15%) have dementia. Mechanisms of injury: It has been demonstrated that HD associated circulatory stress and recurrent regional ischemia drives brain injury. The extent of injury is determined by the degree of BP instability during HD. Peritoneal dialysis patients are not subject to the same stress and retain cognitive abilities. The injury is multifactorial, and amenable to HD based intervention. Optimizing dialysis to minimize harm requires understanding the wide range of potential of pathophysiological processes contributing to this injury. Putative components of pathophysiology that might be amenable to intervention include: a) Direct reduction in tissue perfusion is the characteristic consequence of HD driven multi-organ injury. The investigators have directly visualized this in multiple organ beds during dialysis (heart, gut and kidney), and have inferred it in the brain from the development of ischemic based white matter (WM) injury. b) Inflammation drives WM injury.Endotoxin (derived from gut bacteria) is profoundly pro- inflammatory and translocates from intestinal lumen into the circulation during HD treatment directly causing WM inflammation. Daily HD (gentler fluid removal) normalizes endotoxemia and markers of inflammation. c) Release of the excitotoxic neurotransmitter, glutamate, produces injury in ischemia. Plasma levels are lower in HD patients with less ongoing brain injury. Removal of glutamate by dialysis significantly reduces ischemic injury severity and functional consequences. Previous success in protecting the brain during dialysis: The Investigator recently completed a successful multi- centre RCT of cooled dialysis fluid to abrogate WM progressive injury- strongly supporting the integral role that the HD process plays in brain injury. Hemodialysis patients have specific patterns of progressive brain injury: Currently the problem of dialysis induced functionally significant brain injury is typically not well recognized or a focus of care. Leukoaraiosis describes rarefaction of brain WM, typically associated with vascular cognitive impairment. It is universally present in HD patients (even when correcting for BP). Severity of reduction in cognitive function is proportional to the amount of WM injury, with a predominant loss of subcortical functions (executive functioning). The Investigators have previously demonstrated that the signature of the change in fractional anisotropy in dialysis patients was entirely explained by changes in radial diffusivity, rather than axial diffusivity- pathognomonic of a vascular etiology. Urgent need to develop additional interventions: Although dialysis fluid cooling appears to be effective in helping to protect against WM injury, there are limitations. The degree of cooling that can be applied is limited in some patients by cold symptom tolerability and effectiveness has only been tested in patients new to HD. Patients with more established injury may require additional therapies. These need to be suitable for combination with other emerging dialysis based therapies. Ideally they will be universally applicable, independent of dialysis machine type, low-cost, safe, well tolerated, and simple-requiring few healthcare resources to apply. Remote ischemic preconditioning (RIPC): Ischemic conditioning occurs when a transient non-lethal episode of ischemia reduces the effect of a subsequent larger insult. Similar levels of protection can be achieved by applying brief episodes of ischemia (with a BP cuff on a limb) remote from a target organ. Successful clinical studies using RIPC have been performed to provide protection against ischemia in many organs, including acute stroke, and can prevent leukoaraiosis in animal models. RIPC provides protection against HD-induced acute myocardial injury: The investigators have recently completed a pilot RCT demonstrating a RIPC intervention reduced HD-induced acute cardiac injury by 50%, after only a single application. This effect was maintained over a period of 28 days. RIPC was effective, safe and well tolerated. The investigators are currently engaged in a larger Canadian based study to refine the optimum RIPC regime to provide protection against HD-induced cardiac injury. Interim analysis of this study has confirmed similar levels of efficacy in a Canadian population and allowed us to select the maximally effective RIPC regime, for use in the current proposed study. Clear translational pathway: This project is conceived in an integrated framework of new therapeutic target discovery, intervention development and sequential testing of safety and efficacy. The investigators will use clinically relevant surrogate imaging endpoints for rapid evaluation and refinement of candidate intervention, prior to large-scale testing with survival-based endpoints. The Investigators have already developed a prototype phase III equivalent study. MY-TEMP is an Ontario based cluster randomized study of individualized dialysate cooling (trials registration NCT 02628366), funded in partnership by the Heart and Stroke Foundation, Ontario Ministry of Health and US based large dialysis provider organizations. All 7000 patients will be randomized in Q3 2016. Impact: HD patients characteristically suffer from cognitive impairment. Understanding the mechanisms behind this will allow the development of therapies integrated into dialysis treatment delivery (anti-ischemic, but potentially also directed at issues such as inflammation and dialyzable injury factors), helping patients maintain cognitive vitality, independence and maximize quality of life.
- Conditions
- Chronic Kidney Disease
- Being tested
- Intervention Arm, Control Arm
- Keywords
- Dialysis, Hemodialysis, Remote Ischemic Preconditioning
- Medical subject headings
- Renal Insufficiency, Chronic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Intervention ArmOther
RIPC stimulus will be applied prior to the first intervention visit, using a previously validated (for cardiac protection in HD patients) standard dose (four cycles of cuff inflation to the lower limb of the patient and inflating at 200mmHg for five minutes, with five minutes' deflation).
Control ArmOther
Sham procedure in which the blood pressure cuff will be applied to the lower limb and inflated to 40mmHg for five minutes and deflated for five minutes with the cycle repeated a total of four times prior to dialysis. To be administered on a monthly basis from the baseline visit to the year 1 visit.
| Study group | Role | What they receive |
|---|---|---|
| Intervention Arm | Experimental | RIPC stimulus will be applied prior to the first intervention visit, using a previously validated (for cardiac protection in HD patients) standard dose (four cycles of cuff inflation to the lower limb of the patient and inflating at 200mmHg for five minutes, with five minutes' deflation). To be administered on a monthly basis from the baseline visit to the year 1 visit. Receives: Other: Intervention Arm |
| Control Arm | Sham comparator | Sham procedure in which the blood pressure cuff will be applied to the lower limb and inflated to 40mmHg for five minutes and deflated for five minutes with the cycle repeated a total of four times prior to dialysis. To be administered on a monthly basis from the baseline visit to the year 1 visit. Receives: Other: Control Arm |
What is being measured
The primary outcome is the main question the study is designed to answer.
Neuro-protection against functionally significant new brain injury
Change from baseline in brain damage as observed by progressive ultrastructural white matter changes on MRI imaging.
Measured: 1 year
Secondary outcomes (16)
Brain Perfusion
Change of brain perfusion from baseline MRI.
Measured: 1 year
Excitotoxic neurotransmitter release
Change in Exitotoxic neurotransmitter release from baseline as seen on the combined MRI.
Measured: 1 year
Microglial Inflammation
Change in microglial Inflammation from baseline as seen on the combined MRI.
Measured: 1 year
Neurological impact
Compare observed brain injury, as determined by MRI, to results on neurocognitive test.
Measured: 1 year
Depression scoring
Compare observed brain injury, as determined by MRI, to results on depression scoring test.We will be utilizing the PHQ-9(Patient Health Questionnaire) which is used for screening, diagnosing, monitoring, and measuring the severity of depression. This test consists of 9 questions regarding symptoms which factor into the scoring severity index. Each question is given a score from 0-3, which represents responses such as: not at all(0), several days(1), more than half the days (2), and nearly everyday(3). The scores can be interpreted as follows: 5-9 (minimal symptoms), 10-14 (Minor depression, mild), 15-19 (major depression, moderately severe), and >20 (major depression, severe).
Measured: 1 year
Daily activities
Compare observed brain injury, as determined by MRI, to results on evaluation of activities of daily living survey.
Measured: 1 year
Blood work- blood count
1 year results will be compared to baseline.
Measured: 1 year
Blood work-urea
1 year results will be compared to baseline.
Measured: 1 year
Blood work-microparticles
1 year results will be compared to baseline.
Measured: 1 year
Blood work-Cardiac biomarkers (Troponin T, nTproBNP)
1 year results will be compared to baseline.
Measured: 1 year
Blood work-CRP (C-Reactive Protein)
1 year results will be compared to baseline.
Measured: 1 year
Blood work-glucose
1 year results will be compared to baseline.
Measured: 1 year
Blood work- lactate
1 year results will be compared to baseline.
Measured: 1 year
Blood work- electrolytes
1 year results will be compared to baseline.
Measured: 1 year
Echocardiogram
Correlated to brain perfusion as well as circulatory stress outputs obtained by the CVInsight devices.
Measured: 1 year
CVInsight
Help us to understand if the CVInsight® Patient Monitoring \& Informatics System can be a predictor of organ perfusion
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Nov 2017
- Study start8 Jan 2018
- Primary completion3 Oct 2022
- Study completion12 Oct 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Chronic Kidney DiseaseStudies of the same condition, open and under way.
- More trials run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph'sThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 25 participants (actual)
Sponsor and investigators
- Lead sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Chris McIntyre, London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
- Investigators
- Christopher McIntyre, MD, Principal investigator, London Health Sciences Centre
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03342183
- Sponsor's protocol ID
- 109413
- Status last verified
- Oct 2022
- First submitted
- 16 Oct 2017
- Last updated
- 18 Oct 2022
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Anazodo UC, Wong DY, Theberge J, Dacey M, Gomes J, Penny JD, van Ginkel M, Poirier SE, McIntyre CW. Hemodialysis-Related Acute Brain Injury Demonstrated by Application of Intradialytic Magnetic Resonance Imaging and Spectroscopy. J Am Soc Nephrol. 2023 Jun 1;34(6):1090-1104. doi: 10.1681/ASN.0000000000000105. Epub 2023 Mar 9.
PubMed 36890644
Study at a glance
From the registry record, last updated by the sponsor on 18 Oct 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Reducing Hemodialysis Induced Recurrent Brain Injury to Improve Patients' Lives
- ClinicalTrials.gov ID
- NCT03342183
- Acronym / sponsor ID
- 109413
- Conditions
- Chronic Kidney Disease
- Keywords
- Dialysis, Hemodialysis, Remote Ischemic Preconditioning
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 25 participants (actual)
- Lead sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph'sUniversity, hospital or other
- Study start
- 8 Jan 2018 (actual)
- Primary completion
- 3 Oct 2022 (actual)
- Study completion
- 12 Oct 2022 (actual)
- First posted
- 14 Nov 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Patients who receive dialysis for kidney failure suffer severe cognitive impairment. Hemodialysis causes circulatory stress and ischemia, which causes severe brain injury. It has been demonstrated that a procedure known as Remote Ischemic Preconditioning(RIPC), which involves wrapping a blood pressure cuff around a patient's leg and inflating has the potential of protecting many organs, such as the heart from the effects of dialysis. Our study aims to investigate this phenomenon to determine the extent to which it provides protection to a dialysis patient's brain.
Detailed description
Hemodialysis patients suffer severe cognitive impairment: Abnormalities of cognitive impairment (predominately sub-cortical defects in executive decision making) are almost universal in hemodialysis (HD) patients and appear early after starting dialysis. Around 75% of patients exhibit mild cognitive impairment (MCI) and a high proportion (˜15%) have dementia. Mechanisms of injury: It has been demonstrated that HD associated circulatory stress and recurrent regional ischemia drives brain injury. The extent of injury is determined by the degree of BP instability during HD. Peritoneal dialysis patients are not subject to the same stress and retain cognitive abilities. The injury is multifactorial, and amenable to HD based intervention. Optimizing dialysis to minimize harm requires understanding the wide range of potential of pathophysiological processes contributing to this injury. Putative components of pathophysiology that might be amenable to intervention include: a) Direct reduction in tissue perfusion is the characteristic consequence of HD driven multi-organ injury. The investigators have directly visualized this in multiple organ beds during dialysis (heart, gut and kidney), and have inferred it in the brain from the development of ischemic based white matter (WM) injury. b) Inflammation drives WM injury.Endotoxin (derived from gut bacteria) is profoundly pro- inflammatory and translocates from intestinal lumen into the circulation during HD treatment directly causing WM inflammation. Daily HD (gentler fluid removal) normalizes endotoxemia and markers of inflammation. c) Release of the excitotoxic neurotransmitter, glutamate, produces injury in ischemia. Plasma levels are lower in HD patients with less ongoing brain injury. Removal of glutamate by dialysis significantly reduces ischemic injury severity and functional consequences. Previous success in protecting the brain during dialysis: The Investigator recently completed a successful multi- centre RCT of cooled dialysis fluid to abrogate WM progressive injury- strongly supporting the integral role that the HD process plays in brain injury. Hemodialysis patients have specific patterns of progressive brain injury: Currently the problem of dialysis induced functionally significant brain injury is typically not well recognized or a focus of care. Leukoaraiosis describes rarefaction of brain WM, typically associated with vascular cognitive impairment. It is universally present in HD patients (even when correcting for BP). Severity of reduction in cognitive function is proportional to the amount of WM injury, with a predominant loss of subcortical functions (executive functioning). The Investigators have previously demonstrated that the signature of the change in fractional anisotropy in dialysis patients was entirely explained by changes in radial diffusivity, rather than axial diffusivity- pathognomonic of a vascular etiology. Urgent need to develop additional interventions: Although dialysis fluid cooling appears to be effective in helping to protect against WM injury, there are limitations. The degree of cooling that can be applied is limited in some patients by cold symptom tolerability and effectiveness has only been tested in patients new to HD. Patients with more established injury may require additional therapies. These need to be suitable for combination with other emerging dialysis based therapies. Ideally they will be universally applicable, independent of dialysis machine type, low-cost, safe, well tolerated, and simple-requiring few healthcare resources to apply. Remote ischemic preconditioning (RIPC): Ischemic conditioning occurs when a transient non-lethal episode of ischemia reduces the effect of a subsequent larger insult. Similar levels of protection can be achieved by applying brief episodes of ischemia (with a BP cuff on a limb) remote from a target organ. Successful clinical studies using RIPC have been performed to provide protection against ischemia in many organs, including acute stroke, and can prevent leukoaraiosis in animal models. RIPC provides protection against HD-induced acute myocardial injury: The investigators have recently completed a pilot RCT demonstrating a RIPC intervention reduced HD-induced acute cardiac injury by 50%, after only a single application. This effect was maintained over a period of 28 days. RIPC was effective, safe and well tolerated. The investigators are currently engaged in a larger Canadian based study to refine the optimum RIPC regime to provide protection against HD-induced cardiac injury. Interim analysis of this study has confirmed similar levels of efficacy in a Canadian population and allowed us to select the maximally effective RIPC regime, for use in the current proposed study. Clear translational pathway: This project is conceived in an integrated framework of new therapeutic target discovery, intervention development and sequential testing of safety and efficacy. The investigators will use clinically relevant surrogate imaging endpoints for rapid evaluation and refinement of candidate intervention, prior to large-scale testing with survival-based endpoints. The Investigators have already developed a prototype phase III equivalent study. MY-TEMP is an Ontario based cluster randomized study of individualized dialysate cooling (trials registration NCT 02628366), funded in partnership by the Heart and Stroke Foundation, Ontario Ministry of Health and US based large dialysis provider organizations. All 7000 patients will be randomized in Q3 2016. Impact: HD patients characteristically suffer from cognitive impairment. Understanding the mechanisms behind this will allow the development of therapies integrated into dialysis treatment delivery (anti-ischemic, but potentially also directed at issues such as inflammation and dialyzable injury factors), helping patients maintain cognitive vitality, independence and maximize quality of life.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention Arm | Experimental | Other: Intervention ArmRIPC stimulus will be applied prior to the first intervention visit, using a previously validated (for cardiac protection in HD patients) standard dose (four cycles of cuff inflation to the lower limb of the patient and inflating at 200mmHg for five minutes, with five minutes' deflation). To be administered on a monthly basis from the baseline visit to the year 1 visit. |
| Control Arm | Sham comparator | Other: Control ArmSham procedure in which the blood pressure cuff will be applied to the lower limb and inflated to 40mmHg for five minutes and deflated for five minutes with the cycle repeated a total of four times prior to dialysis. To be administered on a monthly basis from the baseline visit to the year 1 visit. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Male or Female
- Having hemodialysis treatment at least three times per week
- Must be 18 years old or older.
- Ability to speak and understand English
Key exclusion criteria (7 listed)
- Exposure to hemodialysis for less than 90 days prior to recruitment
- Established severe cognitive impairment (Montreal Cognitive Assessment test (MoCA) of less than 18 or with a formal diagnosis of dementia)
- Previous clinical stroke
- Taking drugs to blunt response to RIPC (e.g. ciclosporin, ATP-sensitive potassium channel directed drugs)
- Dialysing using lower limb vascular access
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Intervention ArmRIPC stimulus will be applied prior to the first intervention visit, using a previously validated (for cardiac protection in HD patients) standard dose (four cycles of cuff inflation to the lower limb of the patient and inflating at 200mmHg for five minutes, with five minutes' deflation). | Other | Intervention Arm |
| Control ArmSham procedure in which the blood pressure cuff will be applied to the lower limb and inflated to 40mmHg for five minutes and deflated for five minutes with the cycle repeated a total of four times prior to dialysis. To be administered on a monthly basis from the baseline visit to the year 1 visit. | Other | Control Arm |
Primary outcome
Neuro-protection against functionally significant new brain injury
Time frame: 1 year
Change from baseline in brain damage as observed by progressive ultrastructural white matter changes on MRI imaging.
16 secondary outcomes
Brain Perfusion
Time frame: 1 year
Excitotoxic neurotransmitter release
Time frame: 1 year
Microglial Inflammation
Time frame: 1 year
Neurological impact
Time frame: 1 year
Depression scoring
Time frame: 1 year
Daily activities
Time frame: 1 year
Blood work- blood count
Time frame: 1 year
Blood work-urea
Time frame: 1 year
Blood work-microparticles
Time frame: 1 year
Blood work-Cardiac biomarkers (Troponin T, nTproBNP)
Time frame: 1 year
Blood work-CRP (C-Reactive Protein)
Time frame: 1 year
Blood work-glucose
Time frame: 1 year
Blood work- lactate
Time frame: 1 year
Blood work- electrolytes
Time frame: 1 year
Echocardiogram
Time frame: 1 year
CVInsight
Time frame: 1 year
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Oct 2022.
- Derived from this study: PubMed 36890644Anazodo UC, Wong DY, Theberge J, Dacey M, Gomes J, Penny JD, van Ginkel M, Poirier SE, McIntyre CW. Hemodialysis-Related Acute Brain Injury Demonstrated by Application of Intradialytic Magnetic Resonance Imaging and Spectroscopy. J Am Soc Nephrol. 2023 Jun 1;34(6):1090-1104. doi: 10.1681/ASN.0000000000000105. Epub 2023 Mar 9.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Christopher McIntyre, MD principal investigator
London Health Sciences Centre
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Intervention Arm in people with Chronic Kidney Disease, run by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's at 1 site in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 18 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Neuro-protection against functionally significant new brain injury (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03342183, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Oct 2022.