NCT05016986

Completed

Penetrating Gunshot Injuries at a Single Johannesburg Centre

University of Witwatersrand, South Africa Source

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Other study identifiers

Sponsor study identifier

M180550

Study Type

observational

Actual enrollment (reported)

40

Locations

1 country

Sites

2

Timeline

Study Start

January 1, 2008

Actual (reported)

Primary Completion

December 31, 2018

Actual (reported)

Study Completion

June 30, 2019

Actual (reported)

Brief Summary

A retrospective audit of cardiac penetrating cardiac injuries with specific reference to GSW

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 40 participants
Study completion date: June 30, 2019
Actual (reported)
Listed locations: 1 countries · 2 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
January 1, 2008
Actual (reported)
Primary Completion
December 31, 2018
Actual (reported)
Study Completion
June 30, 2019
Actual (reported)
First Submitted
August 16, 2021
Actual (reported)
First Posted
August 23, 2021
Actual (reported)

Last Updated: August 23, 2021
Status Verified: August 2021
Last Update Submitted: August 20, 2021

Conditions

Trauma

Keywords

cardiacpenetratingGSW

Outcome Measures

Primary Outcomes (2)

Injury patterns (check list)
Document cardiac injuries noted in the study group
01 Jan 2008 till 31 December 2018
The number of in-hospital patients who survive the injury
01 jan 2008 till 31 December 2018

Interventions

Standard clinical managementOther

outcomes in GSW cardiac injuries

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersNo

Age GroupsAdult (18-64), Older Adult (65+)

Sampling MethodNon-Probability Sample

Study Population

Trauma patients who sustained GSW to chest with cardiac injuries in a sigle centre

You may qualify if:

all adult Priority 1 patients with GSW cardiac injuries seen at a Johannesburg Trauma facility

You may not qualify if:

Sponsors & Collaborators

University of Witwatersrand, South Africa
Otherlead

Study Sites (2)

Charlotte Maxeke Johanneburg Academic Hospital

Johannesburg, Gauteng, 2193, South Africa

Charlotte Maxeke Johanneburg Academic Hospital

Johannesburg, Gautheng, 2193, South Africa

MeSH Terms

Conditions

Wounds and Injuries

Study Officials

Maeyane Moeng, MBBCH, FCS
University of Witwatersrand, South Africa
PRINCIPAL INVESTIGATOR

Enrollment

40 participants (actual enrollment reported by the registry).

Study Design

Study Type: observational
Observational Model: COHORT
Time Perspective: RETROSPECTIVE
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Prof

Study Record Dates

First Submitted

August 16, 2021

First Posted

August 23, 2021

Study Start

January 1, 2008

Actual (reported)

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Incomplete data or dead on arrival

Contact the study team to confirm eligibility.

Primary Completion

December 31, 2018

Actual (reported)

Study Completion

June 30, 2019

Actual (reported)

Last Updated

August 23, 2021

Record last verified: 2021-08

Source record

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Source: ClinicalTrials.gov.

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Registry identifier: NCT05016986
Data provider: ClinicalTrials.gov
Source updated: 2021-08-23
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:21:45 UTC

Locations

ZA(2)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Primary Completion

Study Completion

First Submitted

First Posted

Conditions

Keywords

Outcome Measures

Primary Outcomes (2)

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (2)

MeSH Terms

Conditions

Study Officials

Enrollment

Study Design

Study Record Dates

Source record

Locations