COVID-19 and Tissue Damage in Vital Organs

NCT ID: NCT04678687

Last Updated: 2021-02-03

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-01-01
• Study Completion Date: 2022-01-01

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:

1. Cases whose treatment process resulted in death will be included in the study.

2. The cases must be confirmed with the diagnosis of COVID-19 by the RT-PCR (real time polymerase chain reaction) test.

3. 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.

Conditions

Covid19; Postmortem Changes

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

COVID-19 group

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

Group Type: OTHER

Liver, lung, heart and kidney biopsy

Intervention Type: PROCEDURE

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

Interventions

Liver, lung, heart and kidney biopsy

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

Intervention Type: PROCEDURE

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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Dokuz Eylul University

OTHER

Sponsor Role: lead

Responsible Party

Mehmet Nuri Yakar

MD, PhD, Research Assistant

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ali N Gökmen, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Dokuz Eylul University, Department of Anaesthesiology and Reanimation, Division of Intensive Care

Mehmet N Yakar, MD, PhD

Role: STUDY_DIRECTOR

Dokuz Eylul University, Department of Anaesthesiology and Reanimation, Division of Intensive Care

Safiye Aktaş, MD, PhD

Role: STUDY_DIRECTOR

Dokuz Eylul University, Oncology Institute, Department of Basic Oncology

Bilgin Cömert, MD, PhD

Role: STUDY_DIRECTOR

Dokuz Eylul University, Department of Internal Medicine, Division of Intensive Care

Begüm Ergan, MD, PhD

Role: STUDY_DIRECTOR

Dokuz Eylul University, Department of Chest Disease, Division of Intensive Care

Bişar Ergün, MD, PhD

Role: STUDY_DIRECTOR

Dokuz Eylul University, Department of Internal Medicine, Division of Intensive Care

Fırat Bayraktar, MD, PhD

Role: STUDY_CHAIR

Dokuz Eylul University, Department of Internal Medicine, Division of Endocrinology and Metabolism

Eyüp S Uçan, MD, PhD

Role: STUDY_CHAIR

Dokuz Eylul University, Department of Chest Disease

Aylin Erol

Role: STUDY_CHAIR

Dokuz Eylul University, Oncology Institute

Özde E Gökbayrak

Role: STUDY_CHAIR

Dokuz Eylul University, Oncology Institute

Locations

Dokuz Eylul University

Izmir, Balçova, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

COVID-19.PMB

Identifier Type: -

Identifier Source: org_study_id