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The Impact of COVID-19 Pandemic to Trauma Patients in Emergency Department: A Multicenter Experience of Istanbul

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04479124
Recruitment Status : Completed
First Posted : July 21, 2020
Last Update Posted : July 21, 2020
Sponsor:
Information provided by (Responsible Party):
Ramazan Guven, Kanuni Sultan Suleyman Training and Research Hospital

Brief Summary:
COVID-19, which emerged in China in December 2019, has become a pandemic with its spread to many countries of the world. The aim of this multi-centered study is to guide for the approach, organization, diagnosis and treatment of the patients admitted due to trauma to emergency department during the pandemic period.

Condition or disease Intervention/treatment
Trauma Covid19 Diagnostic Test: COVID-19 PCR

Detailed Description:
COVID-19, which emerged in China in December 2019, has become a pandemic with its spread to many countries of the world. The investigators hypothesize that since the number of hospital applications expected to be decreased due to trauma during the COVID-19 period, the level of hospital trauma applications changed. Thus, the aim of this multi-centered study is to guide for the approach, organization, diagnosis and treatment of the patients admitted due to trauma to emergency department during the pandemic period.

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Study Type : Observational
Actual Enrollment : 2000 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: The Impact of COVID-19 Pandemic to Trauma Patients in Emergency Department: A Multicenter Experience of Istanbul
Actual Study Start Date : March 10, 2020
Actual Primary Completion Date : June 30, 2020
Actual Study Completion Date : July 14, 2020

Resource links provided by the National Library of Medicine



Intervention Details:
  • Diagnostic Test: COVID-19 PCR
    Nasopharyngeal samples were analyzed by PCR for the detection of Novel Coronavirus 2019 DNA


Primary Outcome Measures :
  1. trauma admissions [ Time Frame: 3 months ]
    within the study period, trauma patients who admitted to any of the seven study centers will be recorded.



Information from the National Library of Medicine

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Ages Eligible for Study:   up to 50 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
The patients who admitted to any of the emergency departments of seven study centers during the pandemic will be evaluated.
Criteria

Inclusion Criteria:

  • accepted to participate with an informed consent
  • trauma patients who admitted to the study centers

Exclusion Criteria:

  • lack of informed consent
  • lack of data

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04479124


Locations
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Turkey
Istanbul Kanuni Sultan Suleyman Training and Research Hospital
Istanbul, Kucukcekmece, Turkey, 34303
Sponsors and Collaborators
Kanuni Sultan Suleyman Training and Research Hospital
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Responsible Party: Ramazan Guven, Proffessor, Kanuni Sultan Suleyman Training and Research Hospital
ClinicalTrials.gov Identifier: NCT04479124    
Other Study ID Numbers: KSSTHR-TPED
First Posted: July 21, 2020    Key Record Dates
Last Update Posted: July 21, 2020
Last Verified: July 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Emergencies
Wounds and Injuries
Disease Attributes
Pathologic Processes