UnknownNot Applicable

Prediction Study of Complications After Severe Trauma

China3,500 participantsStarted 2012-10

Plain-language summary

The purpose of this study is to evaluate a clinically and economically most effective diagnostic algorithm for prediction of post-traumatic complications in a multicenter sample of severe trauma patients.

Who can participate

Age range18 Years – 65 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * age\> 16 years old and \<65 years old * severe trauma patients (AIS ≧3 or ISS≧16) * admission within 48 hours after injury * given and signed informed consent Exclusion Criteria: * died within 48h after injury * being pregnant or lactating * chronic organ dysfunction comorbidities * long-term anticoagulant therapy before injury * presence of immunosuppression before injury

What they're measuring

morbidity rate of complications after trauma (including sepsis and MODS)

Timeframe: patients will be followed for the duration of hospital stay, an expected average of 3 weeks

Trial details

NCT IDNCT01713205

SponsorJiang Jianxin

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2023-12

Contact for this trial

Anqiang Zhang, MD

+86-23-68757402 zhanganqiang@126.com

View on ClinicalTrials.gov More Trauma trials