- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03854591
A Snapshot Study of Patients Affected by Gunshot Related Injuries in Trauma in South Africa (GRIT)
Gunshot Related Injuries in Trauma
Introduction- Gun violence represents an important cause of disability to the working age population in South Africa. It has unrecognised, but undoubtedly significant implications for the health service and patients affected by these injuries.
Aim- To capture the burden of gunshot injury across South Africa and to establish a network of researchers in this field.
Method- A cross-sectional observational study run across South Africa capturing a nationwide picture of burden and complications associated with these injuries. Each centre will participate in a two-week window of patient screening and recruitment. Patients will be followed up at 6 weeks as per routine clinical practice. Data collected will include nature and number of treatments, length of stay, return to work and complications.
Results-Outcome of the study will be disseminated to the participating centres, relevant health boards and published with all contributors across centres recognised.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Injury is a leading cause of death and morbidity in South Africa. It represents 8% of all cause mortality. Death by injury disproportionately affects young working age people who leave behind dependents. Those who survive their injury may suffer long standing disability. However funding for research in injury accounts for less than 1% percent of the research expenditure of the MRC South Africa. This is particularly incongruous as 'injury' was identified by the Essential National Health Research congress as the number 1 priority for the MRC as far back as 1996.
Causes of injury include work related injury, road accidents and interpersonal violence. Within interpersonal violence, gunshot injuries are a particularly lethal and disabling. South Africa has the 18th highest number of gun owners in the world. However it has a gun homicide rate of 8.2 per hundred thousand. This is comparable to the United States, which has the highest levels of gun ownership anywhere in the world.
This is also the highest number anywhere in Southern Africa. It places South Africa amongst some of the most violent countries in the world such as Honduras and Brazil.
The legacy of gun injuries can be just as devastating to communities with persistent disability and escalating feuds. The health impact of gun related injury has been explored in a few specific centres however the broader national picture remains unclear (4). It seems likely that specific areas will bear most of the gun problem. If this can be sufficiently understood specific interventions resources and expertise can be most appropriately deployed.
RATIONALE FOR CURRENT STUDY Gunshot related injuries are an important cause of mortality and morbidity. In South Africa, this burden is under studied and relatively unique. Most studies focus on death as an outcome for gun related violence, however injuries to limbs as seen by orthopaedic teams are rarely fatal. Unfortunately such injuries are highly significant and cause long term disability for patients. Gunshot injuries are also very resource intensive to treat.
Injury is a significant research priority for South Africa, but currently it receives little funding. There are also no structures in place to study injury and its treatment on a nationwide basis.
This study seeks to build such a network around the clinical problem of gunshot injury. In turn this will act as a platform to deliver big and important clinical effectiveness research for future generations of South African patients.
STUDY OBJECTIVES Primary- To capture on a nationwide basis the burden of orthopaedic gunshot injury in patients.
Secondary- To establish a research collaborative network for Orthopaedic trauma across South Africa.
STUDY METHOD A snap shot cohort study run across participating sites in South Africa. All sites in South Africa offering orthopaedic care have been invited to participate. Each will return anonymised routine data on patients who meet the eligibility criteria over a two week study window. Each patient will be approached for consent as detailed below.
Once open each site will be responsible for recording each patient that meets the inclusion criteria that is referred to the trauma and orthopaedic service.
Outcomes collected will aim to inform both patient level and healthcare system costs in terms of burden of work and legacy of injury.
Each patient will have a unique alphanumeric study number. Against this anonymous identifier, the site data collector(s) will record the data on a secure web based database (REDCap). This safe and secure method will return data to the study coordinating centre.
Consent Each patient will be approached and consent to participate sought. This will cover their agreement to have data recorded; to answer additional questions related to the research objectives both at admission and at follow up. Consent forms will be stored locally. Where patients lack capacity to consent on admission, they will be recorded on the study screening log anonymously. For the duration of their inpatient stay, the clinical team will assess them for recovery of capacity. If the patient dies or fails to recover then only the anonymous screening log data will be recorded in the study. A final attempt to recruit the patient will be made at the 6 week follow up appointment.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Western Cape
-
Cape Town, Western Cape, South Africa, 7925
- Groote Schuur Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Any gunshot related injury presenting to registered study hospital's orthopaedic service.
Exclusion Criteria:
- Isolated injuries to the head, chest or abdomen
- Patients under 18 years of age
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Gunshot related injury
Patients admitted to orthopaedic trauma service with gunshot related injury
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Destination at discharge
Time Frame: 6 weeks after enrolment to study date
|
Record of alive, dead or discharged
|
6 weeks after enrolment to study date
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of cases
Time Frame: 18/02/2019-04/03/2019
|
Total number of gunshot related injuries admitted at each unit
|
18/02/2019-04/03/2019
|
Return to follow up
Time Frame: 01/04/2019-15/04/2019
|
Number of patients that attend their routine follow up appointment
|
01/04/2019-15/04/2019
|
Number of patients who give consent to additional study questions
Time Frame: 18/02/2019-04/03/2019
|
Each patient with capacity will be asked to give consent to ask additional questions
|
18/02/2019-04/03/2019
|
Health Related Quality of Life
Time Frame: Total study period 18/02/2019-15/04/2019
|
Baseline and follow up HRQOL will be assessed using the EQ5D assessment where patients have given consent
|
Total study period 18/02/2019-15/04/2019
|
Complications
Time Frame: Total study period 18/02/2019-15/04/2019
|
At 6-8 week after index admission window any noted complications will be recorded (including surgical site infection and failure of fixation)
|
Total study period 18/02/2019-15/04/2019
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Simon Graham, FRCS, Liverpool School of Hygiene and Tropical Medicine
- Principal Investigator: Sithombo Maqungo, FCS, UCT
- Principal Investigator: Michael Held, FCS, UCT
- Principal Investigator: Maritz Laubscher, FCS, UCT
- Principal Investigator: James Masters, MRCS, University of Oxford
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 755/2018
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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