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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 October 2015
Main ID:  NCT02303613
Date of registration: 25/11/2014
Prospective Registration: No
Primary sponsor: University Hospital, Linkoeping
Public title: A Validation of Current Hospital Triage Performance System Versus RETTS HTPS
Scientific title: A Validation of Current Hospital Triage Performance System Versus RETTS and Identify Trauma Patient Outcome at Moi Teaching and Referral Hospital, Kenya.
Date of first enrolment: November 2014
Target sample size: 628
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02303613
Study type:  Observational [Patient Registry]
Study design:  Observational Model: Cohort, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
Kenya
Contacts
Name:     Maria Lampi, PhD-cand
Address: 
Telephone:
Email:
Affiliation:  Linkoping University
Key inclusion & exclusion criteria

Inclusion Criteria:

Close to 600 trauma patients of ages 14 and above seen at the ED will be captured. All
patients presenting through the ED will be identified and those who meet the inclusion
criteria will be recruited into the study on a daily basis until close to the 600 patient
records is achieved. Patients will be followed through the ED to the receiving facilities
(wards, ICU, HDU, theatre etc) -

Exclusion Criteria:

Those brought in dead, those below 14 years, revisits, or referred patients will be
excluded The patient records will be traced for the entire period the patient is in the
hospital or until key decisions are made on triage category by the ED or receiving units.

There may be need to follow up patients for longer but since the study has a limited
period, records will have to be made up to 30 days admission for those admitted during the
last month.



Age minimum: 14 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Trauma
Wound and Injuries
Intervention(s)
Other: Mapping
Primary Outcome(s)
Identify and mapping of the current 30 days mortality and morbidity. [Time Frame: 30 days]
Secondary Outcome(s)
Secondary ID(s)
KMC-001
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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