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NCT Number: NCT04521881

Clinical Randomisation of an Anti-fibrinolytic in Symptomatic Mild Head Injury in Older Adults

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

Recruiting

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

St George's Hospital, London, United Kingdom

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 50 years or older (actual or estimated)
  • History or evidence of head injury (e.g. laceration, bruise, swelling or pain in head or face)
  • GCS ≥ 13
  • Has one or more of the following:
  • has or had any impaired consciousness (loss of consciousness, amnesia, or confusion)
  • nausea or vomiting
  • Within 3 hours of injury (do not include if interval cannot be estimated e.g. patient unable to confirm time of fall or patient found on floor after an unwitnessed fall and home alone)
  • Not living in a nursing home, mental health institution or prison
  • Patient will be conveyed to or is admitted to a participating hospital

Exclusion criteria

  • TXA not clearly indicated (e.g. major bleeding) or contraindicated (e.g. suspected stroke)

Treatment and study plan

Tranexamic Acid 500 MG

Drug

given once as an intramuscular injection

Primary outcomes

  1. Emergency department discharge

    Time frame: within 24 hours

    discharge

Secondary outcomes

  1. Intracranial bleeding on CT scan

    Time frame: within 48 hours

    any bleeding on the last scan conducted within 48 hours of randomisation

  2. Head injury related death

    Time frame: within 48 hours

    In-hospital head injury-related death within 48 hours of injury

  3. All cause mortality

    Time frame: within 28 days

    Cause of death will be described

  4. Disability

    Time frame: within 28 days

    The Barthel scale will be used to assess functional disability

  5. Global assessment of ability to self-care

    Time frame: within 28 days

    Scale of 1 to 5

  6. Neurosurgery

    Time frame: within 28 days

    receipt of neurosurgery and type

  7. Days in ICU

    Time frame: within 28 days

    Number of days

  8. Re-admission to hospital

    Time frame: within 28 days

    readmission after discharge

  9. Vascular occlusive events

    Time frame: within 28 days

    pulmonary embolism, myocardial infarction, deep vein thrombosis and stroke

  10. Seizures

    Time frame: within 28 days

  11. Intramuscular injection site reaction

    Time frame: within 28 days

    frequency and type of reactions

  12. Pneumonia

    Time frame: within 28 days

  13. Adverse events

    Time frame: within 28 days

    Any untoward medical occurrence (other than pre-specified outcomes)

  14. Dementia

    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.

  15. Key TBI associated outcomes at 1 year

    Time frame: 1 year

    Incidence of Mood disorders, intracranial bleeding and convulsions

Study contacts

Contact information is provided by the study sponsor or research team.

Haleema Shakur-Still

CONTACT

[email protected]

+4407714139500

Sponsors and collaborators

Lead sponsor

London School of Hygiene and Tropical Medicine

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2026
Study completion
2028
First posted
Aug 21, 2020
Registry last updated
Mar 12, 2026

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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