Skip to content

Prediction Study of Complications After Severe Trauma

Identifying Severe Trauma Patients at High Risk of Post-traumatic Complications

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01713205
Acronym
PSCAT
Enrollment
3500
Registered
2012-10-24
Start date
2012-10-31
Completion date
2023-12-31
Last updated
2022-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Organ Dysfunction Syndrome, Sepsis, Trauma

Keywords

trauma ; sepsis; Multiple Organ Dysfunction Syndrome; Prediction; risk

Brief 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.

Detailed description

Trauma is a major public health problem worldwide, ranking as the fourth leading cause of death. One of the most serious complications of major trauma is sepsis, which often induces sequential multiple organ dysfunction syndrome (MODS). There were still no specific biomarkers to predict the susceptibility of complications and outcomes, which leading to the limited prevention methods and the high mortality rate of severe trauma patients. Previous studies from our and other group have found some sepsis and MODS predictors, including genetic polymorphisms, serum cytokines and cell-surface markers. The purposes of this multi-center observational study is to select biomarkers and evaluate a clinically and economically most effective diagnostic algorithm for prediction of complications in severe trauma patients.

Interventions

None listed

Sponsors

Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
CollaboratorOTHER
Chongqing Emergency Medical Center
CollaboratorOTHER
Huazhong University of Science and Technology
CollaboratorOTHER
Second Affiliated Hospital, School of Medicine, Zhejiang University
CollaboratorOTHER
Kunming general Hospital of Chengdu Military Region
CollaboratorUNKNOWN
The Affiliated Hospital Of Guizhou Medical University
CollaboratorOTHER
Jiang Jianxin
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
morbidity rate of complications after trauma (including sepsis and MODS)patients will be followed for the duration of hospital stay, an expected average of 3 weeks

Secondary

MeasureTime frame
survivalwitnin 30 days and 60 days after injury

Countries

China

Contacts

Primary ContactAnqiang Zhang, MD
zhanganqiang@126.com+86-23-68757402

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026