Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06540768
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-02
Brief Title:
Therapeutic Normothermia in TBI
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Therapeutic Normothermia in the Treatment of Traumatic Brain Injury Trial Feasibility Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
MAMBA-FT
Brief Summary:
This feasibility trial is the first step in testing the hypothesis that maintenance of normal body temperature called therapeutic normothermia TN for 72 continuous hours in traumatic brain injury TBI patients can improve cognitive function The trial aims to answer the following questions
1 Is it feasible to conduct this study Conducting the trial includes the ability to identify and enroll appropriate participants implement TN and collect the required data
2 Can the Creyos Health platform cognitive assessment tool be used to assess and quantify cognitive outcomes in TBI patients
Researchers will address the aforementioned questions by looking at the following factors
1 Identification and enrollment rates of appropriate patients
2 Implementation of the intervention and appropriate data collection while admitted
3 Accurate follow up and continued data collection post-discharge
4 Accessibility and ease of use of the Creyos Health platform cognitive assessment tool
Participants will undergo the following procedure
1 Admission to the Critical Care Trauma Centre through the trauma service
2 Allocation to the intervention or no intervention group
3 Implementation of the intervention or of usual care for a continuous 72 hours
4 Completion of the Creyos Health platform cognitive assessment tool at 3 and 6 months post-discharge from the Critical Care Trauma Centre
1 Is it feasible to conduct this study Conducting the trial includes the ability to identify and enroll appropriate participants implement TN and collect the required data
2 Can the Creyos Health platform cognitive assessment tool be used to assess and quantify cognitive outcomes in TBI patients
Researchers will address the aforementioned questions by looking at the following factors
1 Identification and enrollment rates of appropriate patients
2 Implementation of the intervention and appropriate data collection while admitted
3 Accurate follow up and continued data collection post-discharge
4 Accessibility and ease of use of the Creyos Health platform cognitive assessment tool
Participants will undergo the following procedure
1 Admission to the Critical Care Trauma Centre through the trauma service
2 Allocation to the intervention or no intervention group
3 Implementation of the intervention or of usual care for a continuous 72 hours
4 Completion of the Creyos Health platform cognitive assessment tool at 3 and 6 months post-discharge from the Critical Care Trauma Centre
Detailed Description:
Therapeutic normothermia TN is globally accepted as standard of care in post-cardiac arrest patients to maximize neurologic recovery Both hypothermia and normothermia have been trialed and were noted to prevent the harmful effects of hyperthermia on intracranial pressures and the cardiovascular system Normothermia is favored for its improved cardiovascular hematological immunological and metabolic outcomes In trauma patients specifically hypothermia whether therapeutic or accidental has been shown to result in worse outcomes and increased mortality Despite this therapeutic normothermia has never been purposely applied as a primary intervention in TBI patients
This current study aims to assess the feasibility of conducting a single centre randomized controlled trial of TN versus no TN in traumatic brain injury TBI patients Patients will be screened and enrolled through the trauma service in the Critical Care Trauma Centre CCTC
Patients who consent to enroll in the study will be randomized 11 into either the TN or no TN group Participants allocated to the TN group will immediately commence targeted temperature management for 72 hours with 4 hourly temperature checks and interventions as indicated Participants in the no TN group will proceed with standard of care within CCTC Both groups will be followed at 3 and 6 months post-discharge with cognitive assessments via the Creyos Health platform
The trial will allow the research team to assess appropriate participant identification and enrollment rates ease and limitations of intervention implementation data collection and post-discharge follow up The research team will also assess the accessibility and ease of use of the Creyos Health platform in this patient population In depth primary and secondary outcome measures are outlined elsewhere in the application
This feasibility trial will be the first step in potentially introducing an evidence based intervention that directly targets cognitive outcomes in the TBI patient population group
This current study aims to assess the feasibility of conducting a single centre randomized controlled trial of TN versus no TN in traumatic brain injury TBI patients Patients will be screened and enrolled through the trauma service in the Critical Care Trauma Centre CCTC
Patients who consent to enroll in the study will be randomized 11 into either the TN or no TN group Participants allocated to the TN group will immediately commence targeted temperature management for 72 hours with 4 hourly temperature checks and interventions as indicated Participants in the no TN group will proceed with standard of care within CCTC Both groups will be followed at 3 and 6 months post-discharge with cognitive assessments via the Creyos Health platform
The trial will allow the research team to assess appropriate participant identification and enrollment rates ease and limitations of intervention implementation data collection and post-discharge follow up The research team will also assess the accessibility and ease of use of the Creyos Health platform in this patient population In depth primary and secondary outcome measures are outlined elsewhere in the application
This feasibility trial will be the first step in potentially introducing an evidence based intervention that directly targets cognitive outcomes in the TBI patient population group
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None