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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04813731
Other study ID # 2020-05448
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 12, 2020
Est. completion date June 30, 2022

Study information

Verified date January 2022
Source Region Jönköping County
Contact Katarina Hedin, Ass prof
Phone +46761303619
Email katarina.hedin@rjl.se
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The ongoing corona virus disease 2019 (COVID-19) is a viral acute respiratory tract infection caused by server acute respiratory syndrom coronavirus typ 2 (SARS-CoV-2). The signs and symptom of SARS-CoV-2 infection vary and most people with COVID-19 experience illness of mild or moderate severity and recover with symptomatic treatment outside of hospital. Studies have found that some people experience lingering/long-lasting symptoms and only a minority of patients were completely free from COVID-19 related symptoms after two months. About one third still had up to two residual symptoms and 55% had three or more. As far as we know no study on lingering symptoms has been published in patients after a mild or moderate infection managed in primary care settings. The aim of this study is to explore the course of disease over a one year period and describe lingering symptoms and their impact on well-being and daily activities in adult non-hospitalized patients with previous established COVID-19 infection.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date June 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Confirmed SARS-CoV-2 infection, either by polymeras chain reaction (PCR), or by antigen testing (if authorized/recommended/used by national/local governments) - Symptoms consistent with mild to moderate COVID-19 - Maximum of 2 weeks since positive SARS-CoV-2 test - Aged 18 years and older - Patient able and willing to comply with monthly phone calls. Exclusion Criteria: - Hospitalisation due to COVID-19

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Belgium Centre for General Practice, Department of Family Medicine & Population Health (FAMPOP), Faculty of Medicine and Health Sciences, University of Antwerp Antwerp
Belgium the Academic Centre for General Practice (ACHG), Department of Public Health and Primary Care, KU Leuven Leuven
Denmark Center for General Practice at Aalborg University Aalborg
France Département de Santé Publique, Université Côte d'Azur, Centre Hospitalier Universitaire de Nice, Nice, France Nice
Georgia R. Lugar Center for Public Health Research Tbilisi
Germany Institut für Allgemeinmedizin Universitätsklinikum Würzburg Josef-Schneider-Str. 2/D7 97080 Würzburg Würzburg
Ireland School of Medicine, National University of Ireland Galway
Italy Covid-19 primary care special unit Sassuolo, Azienda Unità Sanitaria locale di Modena, Modena, Italy Modena
Netherlands Julius Center, University Medical Center Utrecht Utrecht
Poland Medical University of Lodz, Lodz Lódz
Romania Balan Medfam SRL Cluj Napoca
Sweden Wetterhälsan Primary Health Care Centre Jönköping
Sweden Kärna Primary Health Care Centre Linköping

Sponsors (4)

Lead Sponsor Collaborator
Katarina Hedin National University of Ireland, Galway, Ireland, Research Unit of General Practice, Aalborg, Utrecht University

Countries where clinical trial is conducted

Belgium,  Denmark,  France,  Georgia,  Germany,  Ireland,  Italy,  Netherlands,  Poland,  Romania,  Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time to full recovery symptoms Number of weeks until "back to normal" through study completion, a maximum of 1 year
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