Polytrauma Clinical Trial
Official title:
Effectiveness of ELLASI Intervention Towards Response Time, Deterioration, and Metabolic Status of Polytrauma Patients in the Emergency Department
This clinical trial aims to test the effectiveness of ELLASI intervention in response time, deterioration score, and metabolic status of polytrauma patients in the emergency department. The main questions it aims to answer are: 1. Is the response time of polytrauma patients who receive ELLASI in the intervention group faster than the control group? 2. Is the deterioration score of polytrauma patients who receive ELLASI in the intervention group better than the control group? 3. Is the metabolic status of polytrauma patients who receive ELLASI in the intervention group better than the control group? Polytrauma patients in the intervention group will receive ELLASI, a structured intervention consisting of the six following: 1. Evaluation of airway and cervical control, remove the foreign body, fluid, etc., from the airway, 2. Patient positioning and giving oxygen, head-up, 3. Stabilisation, including IV insertion, applying pressure and bandage, place monitor, and haemodynamic monitoring 4. Assessment: re-assessment of pain and other main complaints 5. Make sure informed consents are documented 6. Inform patient and family for further intervention Polytrauma patients in the control group will receive the usual/standard intervention. Response time, early warning score, and arterial blood gas of polytrauma patients from both groups will be obtained and documented before and after the intervention.
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT03730688 -
Non-invasive Limb Compartment Pressure Measurement
|
N/A | |
| Not yet recruiting |
NCT05544773 -
Comparing Trauma Severity Scores Injury Severity Score "ISS", Rapid Emergency Medicine Score "REMS" and Kampala Trauma Score "KTS"
|
||
| Completed |
NCT04107818 -
Comparison of Viscoelastic Measurement by ROTEM® Delta and ClotPro® in Trauma Patients.
|
||
| Completed |
NCT03780894 -
Transfusion of Red Blood Cells, Tranexamic Acid and Fibrinogen Concentrate for Severe Trauma Hemorrhage at Pre-hospital Phase of Care.
|
Phase 1/Phase 2 | |
| Completed |
NCT01193686 -
Peer Visitation for OEF/OIF Veterans
|
N/A | |
| Active, not recruiting |
NCT03098459 -
Illuminating Neuropsychological Dysfunction and Systemic Inflammatory Mechanisms Gleaned After Hospitalization in Trauma-ICU Study
|
||
| Completed |
NCT03588767 -
Endocrine Response of the Organism to Polytrauma
|
N/A | |
| Suspended |
NCT00555126 -
Forced Air Versus Endovascular Warming in Polytrauma Patients
|
Phase 4 | |
| Not yet recruiting |
NCT04766944 -
Incidence and Associated Risk Factors of ARC in the Trauma Critically Ill Older Than 50 Years Old
|
||
| Recruiting |
NCT05794256 -
Genderspecific Differences in Hormone Levels After Trauma
|
||
| Suspended |
NCT03066817 -
Vitamin D and Bone Homeostasis in Ortho Polytrauma Patients
|
Phase 1/Phase 2 | |
| Completed |
NCT04410952 -
Pelvic Binder vs. Pelvic C-clamp for Bleeding Control
|
||
| Not yet recruiting |
NCT05954936 -
Trauma Registry in Villavicencio, Colombia
|
||
| Completed |
NCT04335838 -
Age, Traumatic Brain Injury and Injury Severity as Independent Risk Factors for In-Hospital Mortality in Polytrauma Patients.
|
||
| Completed |
NCT05221476 -
Red Blood Cell Distribution Width and Charlson Comorbidity Indeces in the Frail Polytraumatized Patient.
|
||
| Completed |
NCT04723992 -
25-Year Experience With Polytraumatized Patients in a Level 1 Trauma Center
|
||
| Recruiting |
NCT06305819 -
Effectiveness of a Self-management Program After Traumatic Injury
|
N/A | |
| Active, not recruiting |
NCT06312436 -
The AT-REBOA Target Trial
|
||
| Active, not recruiting |
NCT03218280 -
Oxidative Stress Expression and Metabolic Imbalance in Critically Ill Polytrauma Patients and the Implications of Antioxidant Therapy on Clinical Outcomes
|
N/A | |
| Completed |
NCT05074095 -
Analysis of Urogenital Injuries in Polytraumatized Patients
|