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COVID-19 and Tissue Damage in Vital Organs

Primary Purpose

Covid19, Postmortem Changes

Status
Unknown status
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Liver, lung, heart and kidney biopsy
Sponsored by
Dokuz Eylul University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Covid19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cases 18 years and older than 18 years.
  • Cases diagnosed with COVID-19 confirmed by PCR test.
  • Cases whose treatment resulted in death.
  • Cases that was allowed the participation in the study by signing the informed consent form by their first degree relatives.

Exclusion Criteria:

  • Cases less than 18 years old.
  • Cases for which the diagnosis of COVID-19 could not be confirmed.
  • Cases for which informed consent could not be obtained.
  • Cases whose treatment continues or results in healing.

Sites / Locations

  • Dokuz Eylul University

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

COVID-19 group

Arm Description

Liver, lung, heart and kidney biopsies will be performed on each case in the COVID-19 group.

Outcomes

Primary Outcome Measures

The level of histopathological changes
In lung; alveolar epithelial cell damage, hyaline membrane formation, type 2 pneumocyte hyperplasia, diffuse alveolar damage, fibroblastic proliferation, fibrin accumulation, inflammatory infiltration and the nature of inflammation. In liver; lobular lymphocytic infiltration, centrilobular sinusoidal dilatation. In kidney; diffuse proximal tubule damage, brushed edge loss, non-isometric vacuolar degeneration, necrosis, hemosiderin, pigment cast, capillary plugs, vasculitis, interciliary inflammation, hemorrhage. In heart; acute ischemic injury, vascular pathology, inflammation.

Secondary Outcome Measures

Full Information

First Posted
December 2, 2020
Last Updated
February 2, 2021
Sponsor
Dokuz Eylul University
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1. Study Identification

Unique Protocol Identification Number
NCT04678687
Brief Title
COVID-19 and Tissue Damage in Vital Organs
Official Title
Evaluation of Postmortem Biopsy Specimens of COVID-19 Cases
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
June 1, 2021 (Anticipated)
Study Completion Date
January 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dokuz Eylul University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study will be conducted in Dokuz Eylül University Hospital, COVID-19 (Coronavirus Disease 2019) intensive care unit. Three primary conditions will be sought for participants: Cases whose treatment process resulted in death will be included in the study. The cases must be confirmed with the diagnosis of COVID-19 by the RT-PCR (real time polymerase chain reaction) test. The first-degree relatives must consent for the participation of the subjects in the study by their first-degree relatives. In the study, samples will be taken from the liver, kidney, lung, and heart. The samples will be stored in a protective solution and sent to the pathology unit. The examinations will determine the microscopic damage to these organs caused by COVID-19. Also, the presence of the SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) will be investigated by RT-PCR in tissues. The presence of ACE-2 (angiotensin converting enzyme 2) receptor and SARS-CoV-2 nucleoprotein antibody will be investigated by histochemical examination in tissues.
Detailed Description
The cases whose treatment resulted in death at Dokuz Eylül University Research and Application Hospital Anesthesiology Intensive Care Unit and whose COVID-19 diagnosis was confirmed by the RT-PCR (real time polymerase chain reaction) test and gave written consent to the inclusion of the patient in the study by a first-degree relative will be included in the study. In the study, samples will be taken from 10 cases in total. Age, gender, length of hospital stay, respiratory rate at the time of hospitalization, oxygene saturation on ICU admission and Horwitz ratio on ICU admission will be recorded. Also, the comorbidities of these cases, the interpretation of the computed tomography findings performed at the first admission to the hospital in terms of COVID-19, the RT-PCR results routinely sent for COVID-19 examination will be recorded in the case report form. Besides, all medical and supportive treatments applied during the intensive care treatment will be recorded. Liver and kidney function tests, inflammation and coagulation markers, hemoglobin level , and cardiac markers, which are routinely examined at the patient's admission to the intensive care unit, will be recorded. Postmortem biopsy samples will be performed within 1 hour after the diagnosis of death is confirmed by the patient's doctor. The researchers will perform the procedures in the isolated room prepared for interventional procedures in intensive care. Researchers will wear personal protective equipment (cap, mask, goggles, gloves) before the procedure under the Ministry of Health's instructions. Biopsy specimens will be taken from the lung, liver, heart, and kidney. Heart, liver, and kidney biopsies were performed as a core biopsy with tru-cut needles under ultrasonography guidance; lung biopsy will be performed by passing through the airway using biopsy forceps. Each of the biopsy samples will be placed separately in 10 ml of 10% phosphate-buffered formalin solution. The containers will be disinfected with 80% alcohol. It will be placed in a closed zippered bag and kept at room temperature. It will be delivered to the pathology unit after 24 hours. The procedures as tissue cassette, extended tissue tracing, paraffin blocking, sectioning, and hematoxylin-eosin staining will be performed under biosafety level 2 rules in pathology. The cases will be coded as CVDPM-1... (Coronavirus Disease Postmortem 1...). Case report forms will be shared with researchers who will conduct pathological examination over the internet. Informed consent forms received from patients' relatives will be filed in the COVID-19 Intensive Care Unit. Routine pathology sections will be evaluated in light microscopy according to the following criteria. Lungs; alveolar epithelial cell damage, hyaline membrane formation, type 2 pneumocyte hyperplasia, diffuse alveolar damage, fibroblastic proliferation, fibrin accumulation, inflammatory infiltration, and the nature of inflammation Liver; lobular lymphocyte infiltration, centrilobular sinusoidal dilatation Kidney; diffuse proximal tubule damage, brushed edge loss, non-isometric vacuolar degeneration, necrosis, hemosiderin, pigmented cast, capillary plugs, vasculitis, intercalary inflammation, hemorrhage, Heart; acute ischemic injury, vascular pathology, inflammation Tissues will be tested for the presence of the SARS-CoV-2 virus by RT-PCR test. ACE2 receptor and SARS-CoV-2 nucleoprotein antibody will be examined by immunohistochemistry.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Covid19, Postmortem Changes

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
COVID-19 group
Arm Type
Other
Arm Description
Liver, lung, heart and kidney biopsies will be performed on each case in the COVID-19 group.
Intervention Type
Procedure
Intervention Name(s)
Liver, lung, heart and kidney biopsy
Intervention Description
Liver, lung, heart and kidney biopsies will be performed on each case in the COVID-19 group.
Primary Outcome Measure Information:
Title
The level of histopathological changes
Description
In lung; alveolar epithelial cell damage, hyaline membrane formation, type 2 pneumocyte hyperplasia, diffuse alveolar damage, fibroblastic proliferation, fibrin accumulation, inflammatory infiltration and the nature of inflammation. In liver; lobular lymphocytic infiltration, centrilobular sinusoidal dilatation. In kidney; diffuse proximal tubule damage, brushed edge loss, non-isometric vacuolar degeneration, necrosis, hemosiderin, pigment cast, capillary plugs, vasculitis, interciliary inflammation, hemorrhage. In heart; acute ischemic injury, vascular pathology, inflammation.
Time Frame
in three months after the participant's death

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cases 18 years and older than 18 years. Cases diagnosed with COVID-19 confirmed by PCR test. Cases whose treatment resulted in death. Cases that was allowed the participation in the study by signing the informed consent form by their first degree relatives. Exclusion Criteria: Cases less than 18 years old. Cases for which the diagnosis of COVID-19 could not be confirmed. Cases for which informed consent could not be obtained. Cases whose treatment continues or results in healing.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ali N Gökmen, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Department of Anaesthesiology and Reanimation, Division of Intensive Care
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mehmet N Yakar, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Department of Anaesthesiology and Reanimation, Division of Intensive Care
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Safiye Aktaş, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Oncology Institute, Department of Basic Oncology
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Bilgin Cömert, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Department of Internal Medicine, Division of Intensive Care
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Begüm Ergan, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Department of Chest Disease, Division of Intensive Care
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Bişar Ergün, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Department of Internal Medicine, Division of Intensive Care
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Fırat Bayraktar, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Department of Internal Medicine, Division of Endocrinology and Metabolism
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Eyüp S Uçan, MD, PhD
Organizational Affiliation
Dokuz Eylul University, Department of Chest Disease
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Aylin Erol
Organizational Affiliation
Dokuz Eylul University, Oncology Institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Özde E Gökbayrak
Organizational Affiliation
Dokuz Eylul University, Oncology Institute
Official's Role
Study Chair
Facility Information:
Facility Name
Dokuz Eylul University
City
İzmir
State/Province
Balçova
ZIP/Postal Code
35330
Country
Turkey

12. IPD Sharing Statement

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COVID-19 and Tissue Damage in Vital Organs

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