Polytrauma
Conditions
Brief summary
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.
Interventions
OTHERELLASI
A structured intervention for polytrauma patients
OTHERStandard
Unstructured interventions that are given in everyday practice (standard intervention)
Sponsors
Indonesia University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Polytrauma patients * Have not received medical treatment before
Exclusion criteria
* Canceled registration * Polytrauma patients who are unwilling to participate in the study
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Response time | Immediately before and after the intervention | Documented from the beginning of ELLASI and standard interventions are delivered to the ending. |
| Deterioration score | Immediately before the intervention start and 3 hours after the intervention end | Measured with Early Warning Score system used in the hospital where the data was collected. The scores range from 0 to 14. Higher scores mean deterioration |
| Acidic Level (pH) | Immediately before the intervention start and 3 hours after the intervention end | Measure pH of arterial blood gas |
| Base Excess (BE) | Immediately before the intervention start and 3 hours after the intervention end | Measure BE of arterial blood gas |
| Bicarbonate level (HCO3) | Immediately before the intervention start and 3 hours after the intervention end | Measure HCO3 of arterial blood gas |
Countries
Indonesia
Contacts
Primary ContactNurlaelah
Outcome results
None listed