Tranexamic Acid 500 MG
Druggiven once as an intramuscular injection
NCT Number: NCT04521881
Tranexamic acid (TXA) reduces head injury deaths. The CRASH-4 trial aims to assess the effects of early intramuscular TXA on intracranial haemorrhage, disability, death, and dementia in older adults with symptomatic mild head injury
Interested in participating?
Request Info50 year and older
All sexes
Interventional
Phase 3
St George's Hospital, London, United Kingdom
TXA reduces bleeding by inhibiting the enzymatic breakdown of fibrin blood clots. Results from randomised trials (CRASH-3 and NCT01990768) show that early treatment with TXA (given intravenously) reduces head injury deaths (pooled RR 0.89, 95% CI 0.80-0.99). In the CRASH-3 trial, the reduction in head injury deaths with TXA was largest in patients with mild and moderate head injuries, particularly if patients were treated soon after injury. However, the CRASH-3 trial included mild TBI patients only if they had intracranial bleeding on CT scan. It is uncertain whether the results apply to mild TBI patients more generally. CRASH-4 is a randomised, double blind, placebo-controlled trial in symptomatic mild TBI in about 10,000 older adults. The pilot phase will include about 500 patients. The trial aims to provide reliable evidence about the effects of early intramuscular TXA on intracranial haemorrhage, disability, death, and dementia in older adults with symptomatic mild head injury.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
given once as an intramuscular injection
Time frame: within 24 hours
discharge
Time frame: within 48 hours
any bleeding on the last scan conducted within 48 hours of randomisation
Time frame: within 48 hours
In-hospital head injury-related death within 48 hours of injury
Time frame: within 28 days
Cause of death will be described
Time frame: within 28 days
The Barthel scale will be used to assess functional disability
Time frame: within 28 days
Scale of 1 to 5
Time frame: within 28 days
receipt of neurosurgery and type
Time frame: within 28 days
Number of days
Time frame: within 28 days
readmission after discharge
Time frame: within 28 days
pulmonary embolism, myocardial infarction, deep vein thrombosis and stroke
Time frame: within 28 days
Time frame: within 28 days
frequency and type of reactions
Time frame: within 28 days
Time frame: within 28 days
Any untoward medical occurrence (other than pre-specified outcomes)
Time frame: 1 year
The occurrence of all-cause dementia will be determined 12 months after randomisation. Dementia will be identified through linkage to routinely collected health-care data.
Time frame: 1 year
Incidence of Mood disorders, intracranial bleeding and convulsions
Contact information is provided by the study sponsor or research team.
London School of Hygiene and Tropical Medicine
Other
Intramuscular Tranexamic Acid for the Treatment of Symptomatic Mild Traumatic Brain Injury in Older Adults: a Randomised, Double-blind, Placebo-controlled Trial
Acronym: CRASH-4
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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