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Clinical, Molecular and Functional Biomarkers for PROgnosis, Pathomechanisms and Treatment Strategies of COVID-19 (PROVID) - (PROVID-CAPNETZ)

Clinical, Molecular and Functional Biomarkers for PROgnosis, Pathomechanisms and Treatment Strategies of COVID-19 (PROVID) - (PROVID-CAPNETZ)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04952337
Acronym
PROVID-CAPNETZ
Enrollment
400
Registered
2021-07-07
Start date
2020-10-01
Completion date
2022-07-01
Last updated
2021-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bacterial Pneumonia, COVID-19, Pneumonia Due to H. Influenzae, Pneumonia Due to Other Specified Infectious Organisms, Pneumonia Due to Streptococcus Pneumoniae, Pneumonia in Diseases Classified Elsewhere, Pneumonia, Organism Unspecified, Viral Pneumonia

Keywords

COVID-19, Community-Acquired Pneumonia, CAPNETZ STIFTUNG, CAP, SARS-CoV-2

Brief summary

The pandemic triggered by the new SARS-CoV-2 presents the German health system with previously unknown challenges. There are currently no effective therapies for the treatment of the SARS-CoV-2 lung disease Covid-19. The aim of the joint project PROVID is to draw conclusions from the often very different clinical appearance of infections with the SARS-CoV-2 pathogen in order to improve patient care through targeted clinical management. The effects of infections with the SARS-CoV-2 pathogen are wide-ranging and include a spectrum from symptomlessness to infections of the upper respiratory tract, uncomplicated but also severe pneumonia with lung failure and high mortality. PROVID will first check whether certain host factors determine the severity and / or the course of Covid-19. Research is also being carried out into whether the molecular and clinical values of Covid-19 patients differ from those of patients with pneumonia caused by other pathogens. In addition, it will be tested whether specific molecular markers describe the severity of the disease and are suitable as an aid for targeted therapy for Covid-19. PROVID is an interdisciplinary joint project made up of three sub-projects that are being implemented at three locations (Charitè-Universitätsmedizin Berlin, Universität Leipzig IMISE and CAPNETZ STIFTUNG / Hannover). PROVID is based on three clinical research platforms with a high track record in recruiting patients with high-quality data and biomaterials on the one hand and guideline-changing results on the other hand: CAPNETZ (competence network CAP, since 2002, world's largest database and biobank for CAP), PROGRESS (Pneumonia Research Network on Genetic Resistance and Susceptibility for the Evolution of Severe Sepsis, since 2007) and CAPSyS (systems medicine of community-acquired pneumonia, since 2014). The COVID-19 patients are recruited into 3 different patient cohorts via these 3 research platforms. 1\. PROVID-CAPNETZ, 2. PROVID-PROGRESS, 3. PROVID-CAPSyS.

Detailed description

Infections with the novel Severe Acute Respiratory Syndrome - Coronavirus-2 (SARS-CoV-2) manifest with a broad spectrum of clinical presentations, ranging from asymptomatic to upper respiratory tract infections, uncomplicated pneumonia and severe pneumonia with respiratory failure and high lethality. Despite more than 1.7 Mio. documented infections worldwide, a profound lack of knowledge impedes clinical management and the development of therapies. COVID-19-associated pneumonia and lung injury differ in relevant details from any of the known types of pneumonia that cause respiratory failure, including viral infections like influenza or MERS-CoV. Thus, it is unclear whether specific decision guidelines established for pneumonia are applicable or whether these need to be refined for COVID-19. That is why the PROVID consortium was founded with BMBF funding. The PROVID consortium thus aims to characterize the host- and virusdependent mechanisms associated with the clinical appearance of COVID-19 to improve patient care through advances in risk stratification and clinical management. Specifically, we aim to test the hypotheses that, 1. host factors (transcriptional response/RNA, proteins, antibodies) determine the severity and/or course of COVID-19, 2. molecular and clinical determinants of COVID-19 differ from those previously deciphered in other types of pneumonia and they can be used as molecular predictors for disease progression, 3. specific molecular markers of severe disease can be tested as therapeutic targets for COVID-19. 4. In addition to presently pursued antivirals and immunomodulators, the stabilization of the pulmonary barrier function could establish a third line for an effective therapy. In PROVID we synergistically combine our expertise in the areas of pneumonia and ARDS, infection immunology, molecular and medical virology, lung physiology and endothelial cell biology, experimental lung infection research, statistics and bioinformatics.

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
CollaboratorOTHER
University of Leipzig
CollaboratorOTHER
Hannover Medical School
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 * Radiological proof of infiltrate (primarily chest x-ray or CT) with positive detection of SARS-CoV-2-virus or with no proven infiltrate with positive detection of SARS-CoV-2-virus * Informed consent signed

Exclusion criteria

* Newly diagnosed, active pulmonary tuberculosis within the last 2 months * Simultaneous participation in PROVID-PROGRESS or PROVID-CAPSyS cohort * Participation of the patient in PROVID-PROGRESS or PROVID-CAPSyS cohort at an earlier point in time

Design outcomes

Primary

MeasureTime frameDescription
Determination of the host- and virusdependent mechanisms associated with the clinical appearence of COVID-19up to 1 yearDetermination of specific molecular markers
Determination of the course of COVID-19up to 1 yearHost factors (transcriptional response/RNA, proteins, antibodies) determine the course of COVID-19
Determination of the severity of COVID-19up to 1 yearHost factors (transcriptional response/RNA, proteins, antibodies) determine the severity of COVID-19

Countries

Germany

Contacts

Primary ContactGrit Barten-Neiner
office@capnetz.de+49-(0)511-532-4434

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026