The Assessment of the Prevalence, Clinical Course and Treatment of COVID-19 Complications

Sponsor
Silesian Centre for Heart Diseases (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04453748
Collaborator
Medical Research Agency, Poland (Other), Medical University of Silesia (Other)
200
1
17.7
11.3

Study Details

Study Description

Brief Summary

SAR-Cov-2 infection and its clinical manifestation known as COVID-19 beside the respiratory and lung involvement may include the cardiovascular system, the nervous system and the liver. In the acute phase of the disease, all of these conditions may be life-threatened. As a result, after the acute phase of COVID-19, early complications may be observed, including heart, lungs, brain, muscles and liver. A few papers to date have been reported of myocarditis, ventricular arrhythmias, post-inflammatory changes in the lung and liver, as well as ischemic changes in the brain, diseases of skeletal muscle, which may have adverse prognostic effects. Due to the extent of the pandemic, the severity of the complications and the expected high complications' prevalence in the early post-recovery period, a study was designed to determine the extent of the problem of early complications after COVID-19. Complex cardiological, pulmonary, neurological and hepatological diagnostics are planned, including laboratory, imaging and functional tests. The results obtained, in addition to determining the scale of the problem, will allow the selection of studies that optimally identify patients with early complications. The purpose of this procedure is to enable rapid treatment of diseases that are complications of SARS-COV-2 infection. An additional aspect raised in the project will be the issue of psychiatric disorders (anxiety, depression, post traumatic disorders).

The main three purposes of the study include:
  1. the assessment of prevalence of particular complications after COVID-19.

  2. identification of the demographic and clinical risk factors of COVID-19 complications

  3. determining the diagnostic tests which are sufficient to detect early complications of COVID-19

Condition or Disease Intervention/Treatment Phase
  • Other: Complex diagnostic panel

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Assessment of the Prevalence, Clinical Course and Treatment of COVID-19 Complications
Actual Study Start Date :
Jun 8, 2020
Anticipated Primary Completion Date :
Oct 31, 2021
Anticipated Study Completion Date :
Nov 30, 2021

Arms and Interventions

Arm Intervention/Treatment
COVID-19 convalescents

People who recovered from COVID-19: have no symptoms and no SARS-Cov2 RNA in PCR

Other: Complex diagnostic panel
Complex, multidisciplinary diagnostic panel, including blood, imaging and functional tests.

Outcome Measures

Primary Outcome Measures

  1. Prevalence of COVID-19 complications [2 months]

    Complications include pulmonary, cardio-vascular, neurological, hepatologic and psychiatric disordes that might be linked to the COVID-19. The diagnostic tests: blood tests, transthoracic echocardiography, spirometry, high-resolution computed tomography, neurological examination, liver ultrasonography and elastography, vasular ultrasonography (veins and arteries), psychiatric questionnairies

Secondary Outcome Measures

  1. Assessment of risk factors of COVID-19 complications [2 months]

    Analysis which demographic and clinical parametrs were associated with particular COVID-19 complication. Statistical analysis of relation between clinical parameters before and during COVID19 and the occurence of COVID19 complications

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 120 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. SARS-Cov-2 RNA confirmed by the PCR method in the acute phase of disease.

  2. Presence of the clinical symptoms associated with COVID-19 in the acute phase of disease

  3. Two negative results of SARS-COV-2 PCR test following the 7-day period of quarantine

  4. Informed consent

Exclusion Criteria:
  1. Any symptoms of infection during the quarantine

  2. Lack of patient's consent

  3. Lack of possibility of travelling to the hospital for tests

Contacts and Locations

Locations

Site City State Country Postal Code
1 Silesian Centre for Heart Disease Zabrze Silesia Poland 41-800

Sponsors and Collaborators

  • Silesian Centre for Heart Diseases
  • Medical Research Agency, Poland
  • Medical University of Silesia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mariusz Gasior, Prof., Silesian Centre for Heart Diseases
ClinicalTrials.gov Identifier:
NCT04453748
Other Study ID Numbers:
  • COVID-19 Complications Study
First Posted:
Jul 1, 2020
Last Update Posted:
Sep 30, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Mariusz Gasior, Prof., Silesian Centre for Heart Diseases
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 30, 2020