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Invasive Disease Caused by Group A Streptococcus (GAS) (DICAR)

Invasive Disease Caused by Group A Streptococcus (GAS) - a Prospective Study (DICAR)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03507101
Acronym
DICAR
Enrollment
45
Registered
2018-04-24
Start date
2018-08-01
Completion date
2024-12-31
Last updated
2023-04-14

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

Conditions

Invasive Group A Beta-Haemolytic Streptococcal Disease

Brief summary

The goal of this study is to gain important knowledge on the pathogenesis and prognostic factors in severe invasive group A streptococcal (GAS) infections, as well as the effects of individual characteristics of both the pathogen and the patient on disease severity. The aim is to recruit a minimum of 60 patients from Tampere and Turku University Hospitals in 2-3 years to gather a suitably wide spectrum of manifestations of the disease, and gather genetic, transcriptomic and diagnostic data on both the patients and pathogens in an effort to further our understanding of the pathogenesis of severe invasive GAS disease.

Detailed description

Invasive group A streptococcal (GAS) infection is a severe, life threatening disease. New prognostic markers are needed to better identify patients at risk of severe complications to better improve their care. By advancing understanding of the mechanisms of severe disease, treatments may be found to hinder the processes behind them. It is likely that different individuals react differently to the same microbe. From previous incidence data the investigators have estimated that it will be possible to recruit a minimum of 60 patients over the course of 2-3 years from Tampere and Turku University Hospitals. This sample size should contain a reasonably wide array of infections with varying stages of severity. The investigators will then gather genetic and transcriptomic data on these patients at three time points, as well as salival samples for antibody analysis, and throat cultures to screen for carriage of the pathogen in question. The genome of all the GAS strains obtained from the patients will also be sequenced. From this the investigators hope to derive information pertaining to the interplay of the patients immunologic response and the pathogens inherent characteristics.

Interventions

OTHERNo intervention

No particular intervention or exposure is of particular interest

Sponsors

Turku University Hospital
CollaboratorOTHER_GOV
University of Turku
CollaboratorOTHER
Tampere University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Adult patients who have been diagnosed with invasive group A streptococcal disease and are willing to participate

Exclusion criteria

* Underage patients are excluded

Design outcomes

Primary

MeasureTime frameDescription
Severe invasive GAS diseaseFour month follow upGAS infection leading to death, complications or disability

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026