Pre-hospital Administration of Tranexamic Acid for Moderate and Severe Traumatic Brain Injury
Primary Purpose
Brain Injuries, Traumatic
Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Tranexamic Acid
Sodium chloride
Sponsored by
About this trial
This is an interventional treatment trial for Brain Injuries, Traumatic focused on measuring Traumatic brain injury
Eligibility Criteria
Inclusion Criteria:
- moderate to severe injuries(post-resuscitation scores Glasgow coma score of 4-12)
- age >= 18 year
- non-penetrating TBI in 2 hours onset
Exclusion Criteria:
- patients with coagulopathy
- pregnancy
- receiving any medication which affects haemostasis
- no consenting form
Sites / Locations
- Department of Neurosurgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Tranexamic acid
Sodium chloride
Arm Description
Focused intervention
Placebo control
Outcomes
Primary Outcome Measures
Glasgow Outcome Scale (GOS)
The GOS is five-category scale used for assessing the neurologic outcome after brain injury as follows: 1, death; 2, vegetative state - unable to interact with the environment; 3, severe disability - unable to live independently but able to follow commands; 4, moderate disability - capable of living independently but unable to return to work or school; and 5, good recovery - able to return to work or school. In our statistical analyses, the outcome will be further dichotomized in unfavorable (GOS 1-3) vs favorable (GOS 4-5); the proportion of unfavorable outcome will be compared between groups.
Secondary Outcome Measures
Vascular occlusive events
Vascular occlusive events includes myocardial infarction, stroke, pulmonary embolism, clinical evidence of deep vein thrombosis.
Death
Length of intensive care unit stay
Full Information
NCT ID
NCT02645552
First Posted
December 22, 2015
Last Updated
December 31, 2015
Sponsor
RenJi Hospital
Collaborators
Shanghai Pudong Emergency Center
1. Study Identification
Unique Protocol Identification Number
NCT02645552
Brief Title
Pre-hospital Administration of Tranexamic Acid for Moderate and Severe Traumatic Brain Injury
Official Title
Pre-hospital Administration of Tranexamic Acid for Adults With Moderate and Severe Traumatic Brain Injury: a Randomized, Double-blinded, Placebo-controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
June 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
RenJi Hospital
Collaborators
Shanghai Pudong Emergency Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is a prospective single-centre randomized trial to compare the effect of tranexamic acid versus placebo in the pre-hospital management of patients with moderate and severe traumatic brain injury.
Detailed Description
Traumatic brain injury (TBI) remains a significant public health concern with poor outcome and one of the unmet needs in medical care. Tranexamic acid (TXA) has been shown to reduce blood loss after elective surgery and improve outcomes after traumatic injury due to bleeding without obvious adverse events. In the CRASH-2 Intracranial Bleeding Study, with the nested randomized trial design, the study showed that treatment with TXA within 8 hours of injury was associated with a reduction in haemorrhage growth [adjusted difference, -3.8 ml, 95% confidence interval (CI), -11.5 ml to 3.9 ml], fewer focal ischaemic lesions [adjusted odds ratio (OR) 0.54, 95% CI 0.20 to 1.46] and fewer death (adjusted OR 0.49, 95% CI 0.22 to 1.06) for patients with TBI (Glasgow coma score ≤ 14). The study also provided direction for future research of TXA in TBI, especially for the patients with moderate and severe TBI in whom an intracranial intracranial bleed (defined as the presence of parenchymal, subdural or epidural haemorrhage) is common.
Furtherly, results of the CRASH-2 trial stressed the importance of early adminstration with TXA for trauma patients, with the evidence showing that treatment of TXA within 1 hour post injury could significantly reduce the risk of death, while the benefit did not exist when TXA was administered more than 3 hours after injury. If the use of TXA could be incorporated into the pre-hospital management of TBI, the outcome of traumatically injured patients would be improved in an early stage. Thus, our study sets out to employ a randomized controlled study design, with a sample of 400 patients, to evaluate the efficacy and safety of early use of TXA in the pre-hospital management for moderate and severe TBI.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Injuries, Traumatic
Keywords
Traumatic brain injury
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Tranexamic acid
Arm Type
Experimental
Arm Description
Focused intervention
Arm Title
Sodium chloride
Arm Type
Placebo Comparator
Arm Description
Placebo control
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid
Other Intervention Name(s)
Transamin
Intervention Description
Tranexamic acid 1 gram in 100 ml saline, by intravenous drip over 10 minutes, once patient admitted to the trial on the spot of TBI
Intervention Type
Other
Intervention Name(s)
Sodium chloride
Other Intervention Name(s)
Placebo
Intervention Description
Sodium Chloride solution (0.9%) 1 ml (gram) in 100 ml saline, by intravenous drip over 10 minutes, once patient admitted to the trial on the spot of TBI
Primary Outcome Measure Information:
Title
Glasgow Outcome Scale (GOS)
Description
The GOS is five-category scale used for assessing the neurologic outcome after brain injury as follows: 1, death; 2, vegetative state - unable to interact with the environment; 3, severe disability - unable to live independently but able to follow commands; 4, moderate disability - capable of living independently but unable to return to work or school; and 5, good recovery - able to return to work or school. In our statistical analyses, the outcome will be further dichotomized in unfavorable (GOS 1-3) vs favorable (GOS 4-5); the proportion of unfavorable outcome will be compared between groups.
Time Frame
6 months post injury
Secondary Outcome Measure Information:
Title
Vascular occlusive events
Description
Vascular occlusive events includes myocardial infarction, stroke, pulmonary embolism, clinical evidence of deep vein thrombosis.
Time Frame
6 months post injury
Title
Death
Time Frame
6 months post injury
Title
Length of intensive care unit stay
Time Frame
6 months post injury
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
moderate to severe injuries(post-resuscitation scores Glasgow coma score of 4-12)
age >= 18 year
non-penetrating TBI in 2 hours onset
Exclusion Criteria:
patients with coagulopathy
pregnancy
receiving any medication which affects haemostasis
no consenting form
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Junfeng Feng, MD, PhD
Phone
86-21-68383707
Email
fengjfmail@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yanqing Ni, MD
Phone
86-13601602411
Email
pd120xz@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guoyi Gao, MD, PhD
Organizational Affiliation
Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Neurosurgery, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200127
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Junfeng Feng, MD, PhD
Phone
86-21-68383707
Email
fengjfmail@163.com
First Name & Middle Initial & Last Name & Degree
Yanqing Ni, MD
Phone
86-21-68383707
Email
pd120xz@126.com
First Name & Middle Initial & Last Name & Degree
Guoyi Gao, MD, PhD
First Name & Middle Initial & Last Name & Degree
Yanqing Ni, MD
First Name & Middle Initial & Last Name & Degree
Qing Mao, MD, PhD
First Name & Middle Initial & Last Name & Degree
Junfeng Feng, MD, PhD
First Name & Middle Initial & Last Name & Degree
Jijun Sheng, MD
First Name & Middle Initial & Last Name & Degree
Hua Jiang, MD
First Name & Middle Initial & Last Name & Degree
Junlai Gu, MD
First Name & Middle Initial & Last Name & Degree
Jinghong Yang, MD
First Name & Middle Initial & Last Name & Degree
Xianghui Lu, MD
First Name & Middle Initial & Last Name & Degree
Xianfeng Qin, MD
First Name & Middle Initial & Last Name & Degree
Zhiguo Wang, MD
First Name & Middle Initial & Last Name & Degree
Jingde Xu, MD
First Name & Middle Initial & Last Name & Degree
Hongguan Wang, MD
First Name & Middle Initial & Last Name & Degree
Aiqun Cao, MD
First Name & Middle Initial & Last Name & Degree
Cao Wang, MD
First Name & Middle Initial & Last Name & Degree
Kaizhi Wang, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
20554319
Citation
CRASH-2 trial collaborators; Shakur H, Roberts I, Bautista R, Caballero J, Coats T, Dewan Y, El-Sayed H, Gogichaishvili T, Gupta S, Herrera J, Hunt B, Iribhogbe P, Izurieta M, Khamis H, Komolafe E, Marrero MA, Mejia-Mantilla J, Miranda J, Morales C, Olaomi O, Olldashi F, Perel P, Peto R, Ramana PV, Ravi RR, Yutthakasemsunt S. Effects of tranexamic acid on death, vascular occlusive events, and blood transfusion in trauma patients with significant haemorrhage (CRASH-2): a randomised, placebo-controlled trial. Lancet. 2010 Jul 3;376(9734):23-32. doi: 10.1016/S0140-6736(10)60835-5. Epub 2010 Jun 14.
Results Reference
result
Learn more about this trial
Pre-hospital Administration of Tranexamic Acid for Moderate and Severe Traumatic Brain Injury
We'll reach out to this number within 24 hrs