- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05484947
The HIV Testing Trends and Outcomes at a Johannesburg Trauma ICU Unit
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Trauma ICU admission of 18 years and older were enrolled in the study. The HIV status was further divided into HIV-positive, HIV-negative, and HIV-unknown subgroups. The gender, ages, mechanism of injury, injuries sustained, ISS, physiological data, septic-related complications, and in-hospital mortality were noted and further analyzed.
Descriptive statistics were utilised using STATA version 15, and a p-value of <0.05 was considered statistically significant.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Gauteng
-
Johannesburg, Gauteng, South Africa, 2193
- Charlotte Maxeke Johanneburg Academic Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria: Trauma patients admitted to a Trauma ICU at CMJAH -
Exclusion Criteria: Those under the age of 18 or with incomplete data
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
HIV-positive
Those that were actually tested and had HIV-positive results
|
HIV testing on a voluntary basis
|
|
HIV-Negative
Those tested and had HIV-negative results
|
HIV testing on a voluntary basis
|
|
HIV-Unknown
those who had not volunteered for HIV testing
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The HIV testing trends
Time Frame: study period over two years (from 01 January 2017 till 31 December 2018)
|
Number tested for HIV in the study group
|
study period over two years (from 01 January 2017 till 31 December 2018)
|
|
Outcomes
Time Frame: study period over two years (from 01 January 2017 till 31 December 2018)
|
Septic related complications (wound infections, chest sepsis, septicaemia and sepsis related organ failure incidents
|
study period over two years (from 01 January 2017 till 31 December 2018)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mortality
Time Frame: study period over two years (from 01 January 2017 till 31 December 2018)
|
In-hospital mortality in the cohort
|
study period over two years (from 01 January 2017 till 31 December 2018)
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Witwatersrand
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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