The HIV Testing Trends and Outcomes at a Johannesburg Trauma ICU Unit

July 30, 2022 updated by: Maeyane Stephens Moeng, University of Witwatersrand, South Africa
A retrospective observational study on the HIV testing trend and outcomes in a trauma population admitted to a critical care unit for care.

Study Overview

Status

Completed

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

Observational

Enrollment (Actual)

868

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Gauteng
      • Johannesburg, Gauteng, South Africa, 2193
        • Charlotte Maxeke Johanneburg Academic Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Major Trauma patients admitted to a Trauma unit at a Johannesburg Trauma Unit

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2017

Primary Completion (ACTUAL)

December 31, 2018

Study Completion (ACTUAL)

August 18, 2021

Study Registration Dates

First Submitted

July 23, 2022

First Submitted That Met QC Criteria

July 30, 2022

First Posted (ACTUAL)

August 2, 2022

Study Record Updates

Last Update Posted (ACTUAL)

August 2, 2022

Last Update Submitted That Met QC Criteria

July 30, 2022

Last Verified

July 1, 2022

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)?

UNDECIDED

IPD Plan Description

only with close collaboration of future studies

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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