Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:50 PM
Ignite Modification Date:
2025-12-24 @ 10:50 PM
NCT ID:
NCT02344069
Eligibility Criteria:
Inclusion Criteria:
* Trauma patient received directly from the scene of the accident AND
* Age ≥ 18 years AND
* Initiated order of transfusion of at least one blood component within the 1st hour of arrival AND
* Predicted to need transfusion package therapy during the initial resuscitation (first 2 hours) AND
* Consent obtainable from patient or scientific guardians (independent physicians and/or next of kin
Exclusion Criteria:
* Duration of \> 2 hours from time of accident to arrival at trauma centre OR
* Known anticoagulant treatment (vitamin K antagonist, dabigatran, rivaroxiban, apixaban) OR
* Severe isolated traumatic brain injury OR
* Moribund patient with devastating injuries and expected to die within one hour of admission OR
* Withdrawal from active therapy OR
* Previously, within 30 days, included in a randomized trial, if known at the time of enrolment OR
* Known body weight \< 55 kg OR
* Any blood product prior to inclusion
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02344069
Study Brief:
Protocol Section:
NCT02344069