- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07903727
Medical,Nursing Record,PE, Blood Test and Radiological Examination ,Morality and Mobility of Multiple Trauma Patient (trauma)
Collect Results of Medical and Nursing Record,Physical Examination, Blood Test and Radiological Examination of Multiple Trauma Patients and Activated Trauma Team to Find the Correlation With Patient's Morality and Mobility
This study aims to analyze statistical data on physiological examination values, blood test results, and radiological findings in patients admitted to the emergency department for severe trauma. Given the diverse symptoms and varying mortality rates associated with severe trauma, this research seeks to understand and develop a feasible emergency department assessment model for rapid diagnosis and treatment assessment before the onset of severe trauma patients.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
- This is a single-center retrospective study of patients admitted to the emergency department, primarily reviewing the medical records, emergency room observations, and patient examination findings.
- Starting in August 2025, the investigators collected data from patients who visited the hospital's emergency department from September 2015, focusing on retrospective medical records, hospital observations, and patient examination findings, including statistical analysis of physiological examination values, blood test values, and radiological examination results.
- This data can assist and remind attending physicians in the prognostic diagnosis of similar patients.
- This study will explore specific methods and effectiveness in improving the response of attending physicians to patients admitted with severe trauma.
- The benefits and economics of this operational model to increase the likelihood of accurate diagnosis and timely assessment of patients with severe trauma arriving at the emergency department, while also improving the quality of hospital staff allocation.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Chia-Hsi Chen, physician
- Telefonnummer: 3708 886-5-2756000
- E-mail: stmirb3707@gmail.com
Undersøgelse Kontakt Backup
- Navn: Chung-Jing Wang, professor
- Telefonnummer: 3708 886-5-2756000
- E-mail: stmirb3707@gmail.com
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Patients with severe trauma admitted to the emergency department
Beskrivelse
Inclusion Criteria:
- severe trauma
- admitted to emergency department
Exclusion Criteria:
- incomplete clinical data
- lack of information in their medical records
- non-traumatic patients.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Observationsmodeller: CASE_CONTROL
- Tidsperspektiver: CROSS_SECTIONAL
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
trauma
trauma with fracture, chest, abdomen, blunt |
Collect results of medical and nursing record, physical examination, blood test and radiological examination of multiple trauma patients |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Collect results of trauma patients and find the correlation of patient's morality and mobility
Tidsramme: From enrollment to the end of treatment at 12 weeks
|
Collect results of medical and nursing record, physical examination, blood test and radiological examination of multiple trauma patients and activated trauma team to find the correlation with patient's morality and mobility |
From enrollment to the end of treatment at 12 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studieleder: Chung-Jing Wang, professor, Institutional Review Board St. Martin De Porres Hospital
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 25B-024
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
This is the private medical data
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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