COVID-19 Clinical Trial
— COVERSCANOfficial title:
Mapping Organ Health Following COVID-19 Disease Due to SARS-CoV-2 Infection
| NCT number | NCT04369807 |
| Other study ID # | 20/SC/0185 |
| Secondary ID | |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | April 21, 2020 |
| Est. completion date | April 19, 2022 |
| Verified date | January 2022 |
| Source | Perspectum |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
A prospective, longitudinal, observational cohort study looking at patients following COVID-19 disease using multi-parametric magnetic resonance imaging (MRI) to assess the degree and prevalence of organ injury.
| Status | Completed |
| Enrollment | 693 |
| Est. completion date | April 19, 2022 |
| Est. primary completion date | April 19, 2022 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - Male or female 18 years of age and older willing and able to give informed consent to participate in the study - Recent confirmed diagnosis of SARS-CoV-2 RNA via a polymerase chain reaction (PCR) assay (having been discharged 7 or more days from hospital). Exclusion Criteria: - Symptoms of active respiratory viral infection: - high temperature (over 37.8C/100.04F) - cough (consistent for over an hour; 3 or more episodes in 24 hours) - The participant may not enter the study with any known contraindication to magnetic resonance imaging (including but not limited to pregnancy, a pacemaker or other metallic unfixed implanted device, metallic fragments, extensive tattoos, severe claustrophobia). - Any other cause, including a significant underlying disease or disorder which, in the opinion of the investigator, may put the participant at risk by participating in the study or limit the participant's ability to participate. |
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | Mayo Clinic Healthcare | London | |
| United Kingdom | Gemini | Oxford |
| Lead Sponsor | Collaborator |
|---|---|
| Perspectum |
United Kingdom,
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* Note: There are 25 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Characterise prevalence and severity of organ volume change and damage (heart, kidneys and liver) | In patients recovering from COVID-19 disease:
Characterise using summary statistics the prevalence and severity of organ volume change and damage to heart, kidneys and liver |
12 Months | |
| Secondary | Characterise prevalence and severity of organ volume change and damage (lung, pancreas and spleen) | In patients recovering from COVID-19 disease:
To characterise using summary statistics the prevalence and severity of organ volume change and damage in lung, pancreas and spleen |
12 Months | |
| Secondary | Change from Baseline in liver-specific biomarkers: volume, iron corrected T1(cT1), fat content and T2star | In patients recovering from COVID-19 disease:
Characterise liver damage as assessed by liver volume in liters, iron corrected T1 (cT1) in milliseconds, liver fat content as %, liver T2star in milliseconds (a correlate of liver iron content) |
6 Months | |
| Secondary | Change from Baseline in organ-specific biomarkers characterising organ volume change in the heart and spleen along with organ volume and damage in the kidney, liver and pancreas assessed by volume, iron corrected T1 (cT1) and fat infiltration | In patients recovering from COVID-19 disease:
Characterise heart and spleen damage as assessed by liver volume in liters as well as kidney, liver and pancreas damage as assessed by volume in liters, iron corrected T1 (cT1) in milliseconds, fat infiltration as %, T2star in milliseconds (a correlate of liver iron content). |
12 Months | |
| Secondary | Change in patient reported outcome measured by the Dyspnea-12 questionnaire | In patients recovering from COVID-19 disease:
Change in patient reported outcome measures collected to assess breathlessness and its effect on overall health and daily life assessed by Dyspnea-12. Each question is assigned a value between: none, mild, moderate and severe and is used to assess breathing characteristics. |
12 Months | |
| Secondary | Change in patient reported outcome measured by the Saint George's Respiratory questionnaire (SGRQ) | In patients recovering from COVID-19 disease:
Change in patient reported outcome measures collected to assess breathlessness and its effect on overall health and daily life assessed by the St. George's Respiratory questionnaire. Each section comprises of questions in various formats allowing to assess which aspects of the illness cause the participant the most problems in daily life. There is no score on a scale to communicate the scale title. |
12 Months | |
| Secondary | Change in patient reported outcome measured by the EQ-5D-5L questionnaire | In patients recovering from COVID-19 disease:
Change in patient reported outcome measures collected to assess breathlessness and its effect on overall health and daily life assessed by the EQ-5D-5L questionnaire. Two main sections provide the opportunity to capture statements best describing a participant's daily health and a scale form 0 to 100 capturing self-reported health stats. (100 being the best health imaginable and vice versa) |
12 Months | |
| Secondary | Degree of change in liver MR-derived biomarkers | In patients recovering from COVID-19 disease:
Difference from Baseline in degree of change in liver MR-derived biomarkers with and without known genetic variants associated with liver disease (e.g., PNPLA3) using a paired t-test (or non-parametric alternative) |
12 Months |
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