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 @ 12:42 PM
Ignite Modification Date:
2025-12-24 @ 12:42 PM
NCT ID:
NCT02654561
Eligibility Criteria:
Inclusion Criteria:
* Clinical diagnosis of severe sepsis or/and septic shock
* suspected DIC:the score of Platelets plus International Normalized Ratio in the JAAM criteria is equal or more than 3 scores
Exclusion Criteria:
* consent declined
* pregnant or breastfeeding
* the length during ICU is less than 24 hours
* with other types of shock
* have bleeding or high risk for bleeding
* have an indication for therapeutic anticoagulation
* have a known or suspected adverse reaction to UFH including HIT
* are currently enrolled in another trial
* known or suspected cirrhosis or other severe hepatic diseases
* terminal illness with a life expectancy of less than 28 days
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02654561
Study Brief:
Protocol Section:
NCT02654561