Ignite Creation Date:
2024-05-06 @ 8:08 PM
Last Modification Date:
2024-10-26 @ 3:21 PM
Study NCT ID:
NCT06262061
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-02-15
First Post:
2023-09-21
Brief Title:
Propranolol for the Treatment of Traumatic Brain Injury
Sponsor:
London Health Sciences Centre
Organization:
London Health Sciences Centre
Study Overview
Official Title:
Propranolol for the Treatment of Traumatic Brain Injury
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Traumatic brain injury TBI is a leading cause of global disease and directly affects over 15 million Canadians with 165 000 TBIs occurring yearly in Canada Despite the burden of TBIs there are limited treatment options available and current treatments generally focus on supportive care The aim of TBI treatment is reduce inflammation and damage occurring after the TBI secondary injury
Beta- blockers BBs are medications commonly used to block the actions of endogenous catecholamines- hormones that are thought to contribute to secondary injury within brain tissue This reduces metabolic demand in the vulnerable injured brain BBs have been studied in several retrospective trials and one single-center non- blinded randomized controlled study These results point towards a benefit to the use of BBs in TBI but need to be confirmed in a rigorous manner before they are widely adopted
The current study aims to assess the feasibility of a single centre randomized controlled trial of BBs versus placebo to treat moderate to severe TBI This feasibility trial will inform the planning of a large multi-center study powered to detect a difference in cognitive outcomes and mortality It also will allow the investigators to gather biologic samples for measuring serum catecholamines and inflammatory mediators to better understand the basic science mechanisms of BBs in this patient population and to assess the feasibility of using the Cambridge Battery to assess cognitive outcomes of trial participants
Beta- blockers BBs are medications commonly used to block the actions of endogenous catecholamines- hormones that are thought to contribute to secondary injury within brain tissue This reduces metabolic demand in the vulnerable injured brain BBs have been studied in several retrospective trials and one single-center non- blinded randomized controlled study These results point towards a benefit to the use of BBs in TBI but need to be confirmed in a rigorous manner before they are widely adopted
The current study aims to assess the feasibility of a single centre randomized controlled trial of BBs versus placebo to treat moderate to severe TBI This feasibility trial will inform the planning of a large multi-center study powered to detect a difference in cognitive outcomes and mortality It also will allow the investigators to gather biologic samples for measuring serum catecholamines and inflammatory mediators to better understand the basic science mechanisms of BBs in this patient population and to assess the feasibility of using the Cambridge Battery to assess cognitive outcomes of trial participants
Detailed Description:
Traumatic brain injury is a spectrum of illness ranging from mild concussive symptoms to debilitating and even life-threatening injury Between 2002 and 2016 there were 3550 deaths per year due to TBI Between 2006 and 2018 there were 17 500 hospitalizations per year due to TBI As TBIs often affect youth and working- age adults they are responsible for a very large economic burden costing Canada 73 billion in 2011 and rising to a projected 82 billion in 2031
TBI causes morbidity and morbidity in two phases The primary initial injury results in damage to brain tissue and is only preventable with injury prevention programs The cornerstone of medical TBI management hinges on avoidance of secondary injury to vulnerable brain tissue This translates to supportive care for these patients such as normalization of vital signs blood glucose and treatment of seizures if present Any abnormalities such as low blood pressure or oxygen levels do not provide an appropriate environment for the recovery of brain function and negatively impact recovery There are few targeted medications that can be given in the initial management of TBI patients One of these groups of medications is osmotic agents that help to reduce intracranial pressure in cases of elevated intracranial pressure Osmotic agents such as mannitol or hypertonic saline act transiently and as a bridging therapy to surgical intervention Medications to reduce bleeding such as TXA have been studied but have not been shown to reduce mortality Given the limitations and equivocal role of these medications additional therapies to reduce the devastating sequelae in TBI patients are necessary
Beta-blockers are a class of medications which act on various b adrenergic receptors in the body either b1 or b2 b1 receptors are located primarily in the heart and to a lesser extent the kidneys and adipose tissue while b2 receptors are located in the lungs vasculature and liver Depending on which b receptors are inhibited different beta-blockers exert variable physiologic effects There are non-selective beta-blockers bind to both b1 and b2 as well as selective beta-blockers solely bind to b1 receptors available Propranolol is an example of a non-selective beta-blocker - it will lower heart rate and blood pressure by its cardiac effects on b1 receptors but also acts peripherally Propranolol can uniquely cross the blood-brain barrier and is able to bind to b receptors that are also present in the central nervous system TBI patients commonly develop episodes of elevated heart rate blood pressure and agitation secondary to overactivation of the sympathetic nervous system Administration of beta-blockers helps mitigate these events thereby reducing the metabolic demand in vulnerable injured brain It is because of these mechanisms that propranolol is the beta-blocker that has been postulated to be most beneficial for patients with TBI Blocking these receptors leads to decreased metabolic demand and inflammation in neuronal cells An important objective of this feasibility trial is for the investigator team to collaborate with Dr Allan and her team to measure differences in serum catecholamines and inflammatory mediators between participants in the Propranolol group as compared to the placebo group
There have been several retrospective analyses of patients with TBI on at-home beta-blocker therapy or who received beta-blockers during the course of their hospital stay many of which demonstrated improved outcomes In a meta-analysis combining prospective and retrospective cohorts beta- blocker administration was associated with a reduction in in-hospital mortality The only randomized control study of propranolol in TBI examined early administration of propranolol to TBI patients and its impacts on plasma catecholamine levels and physiologic parameters The authors found lower levels of plasma catecholamines and improved vital signs including Glasgow Coma Scale GCS scores at 7 days This study was unblinded and occurred in a single center and as such is at risk of bias
While most studies of propranolol in TBI have focused on mortality as the outcome of choice this is not ideal for several reasons Mortality is a crude marker of function in TBI whereas functional outcomes are the patient-centered outcome of choice in neurologic injury The Glasgow Outcomes Scale Extended is a validated measure of neurologic function and is the standard for assessment of recovery following neurological injury
Additionally the investigators propose to evaluate the feasibility of using the Cambridge Battery developed by Dr Adrian Owen to evaluate short and longer term cognitive outcomes in trial participants This neuropsychologic measure has been used in a variety of neurologic testing studies evaluating CNS disorders and medication but has not to date been applied to TBI patients This represents an exciting opportunity to develop a new tool for the assessment of the traumatically brain injured patient with the advantage of a strong record of safety and reliability in other populations
In order to change practice an adequately powered multi-center RCT is necessary to evaluate the role of beta-blockers in patients with TBI The investigators propose a feasibility study of beta-blockers in TBI at London Health Sciences Center LHSC as a first step towards a future multi-center RCT
TBI causes morbidity and morbidity in two phases The primary initial injury results in damage to brain tissue and is only preventable with injury prevention programs The cornerstone of medical TBI management hinges on avoidance of secondary injury to vulnerable brain tissue This translates to supportive care for these patients such as normalization of vital signs blood glucose and treatment of seizures if present Any abnormalities such as low blood pressure or oxygen levels do not provide an appropriate environment for the recovery of brain function and negatively impact recovery There are few targeted medications that can be given in the initial management of TBI patients One of these groups of medications is osmotic agents that help to reduce intracranial pressure in cases of elevated intracranial pressure Osmotic agents such as mannitol or hypertonic saline act transiently and as a bridging therapy to surgical intervention Medications to reduce bleeding such as TXA have been studied but have not been shown to reduce mortality Given the limitations and equivocal role of these medications additional therapies to reduce the devastating sequelae in TBI patients are necessary
Beta-blockers are a class of medications which act on various b adrenergic receptors in the body either b1 or b2 b1 receptors are located primarily in the heart and to a lesser extent the kidneys and adipose tissue while b2 receptors are located in the lungs vasculature and liver Depending on which b receptors are inhibited different beta-blockers exert variable physiologic effects There are non-selective beta-blockers bind to both b1 and b2 as well as selective beta-blockers solely bind to b1 receptors available Propranolol is an example of a non-selective beta-blocker - it will lower heart rate and blood pressure by its cardiac effects on b1 receptors but also acts peripherally Propranolol can uniquely cross the blood-brain barrier and is able to bind to b receptors that are also present in the central nervous system TBI patients commonly develop episodes of elevated heart rate blood pressure and agitation secondary to overactivation of the sympathetic nervous system Administration of beta-blockers helps mitigate these events thereby reducing the metabolic demand in vulnerable injured brain It is because of these mechanisms that propranolol is the beta-blocker that has been postulated to be most beneficial for patients with TBI Blocking these receptors leads to decreased metabolic demand and inflammation in neuronal cells An important objective of this feasibility trial is for the investigator team to collaborate with Dr Allan and her team to measure differences in serum catecholamines and inflammatory mediators between participants in the Propranolol group as compared to the placebo group
There have been several retrospective analyses of patients with TBI on at-home beta-blocker therapy or who received beta-blockers during the course of their hospital stay many of which demonstrated improved outcomes In a meta-analysis combining prospective and retrospective cohorts beta- blocker administration was associated with a reduction in in-hospital mortality The only randomized control study of propranolol in TBI examined early administration of propranolol to TBI patients and its impacts on plasma catecholamine levels and physiologic parameters The authors found lower levels of plasma catecholamines and improved vital signs including Glasgow Coma Scale GCS scores at 7 days This study was unblinded and occurred in a single center and as such is at risk of bias
While most studies of propranolol in TBI have focused on mortality as the outcome of choice this is not ideal for several reasons Mortality is a crude marker of function in TBI whereas functional outcomes are the patient-centered outcome of choice in neurologic injury The Glasgow Outcomes Scale Extended is a validated measure of neurologic function and is the standard for assessment of recovery following neurological injury
Additionally the investigators propose to evaluate the feasibility of using the Cambridge Battery developed by Dr Adrian Owen to evaluate short and longer term cognitive outcomes in trial participants This neuropsychologic measure has been used in a variety of neurologic testing studies evaluating CNS disorders and medication but has not to date been applied to TBI patients This represents an exciting opportunity to develop a new tool for the assessment of the traumatically brain injured patient with the advantage of a strong record of safety and reliability in other populations
In order to change practice an adequately powered multi-center RCT is necessary to evaluate the role of beta-blockers in patients with TBI The investigators propose a feasibility study of beta-blockers in TBI at London Health Sciences Center LHSC as a first step towards a future multi-center RCT
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None