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Validation and implementation of rapid testing for SARS-CoV-2 in the primary care setting

Validation and implementation of rapid testing for SARS-CoV-2 in the primary care setting - COVID-19 rapid test in urgent primary care

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49821
Enrollment
1500
Registered
2020-11-26
Start date
2020-12-01
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

Coronavirus Disease 19

Interventions

None listed

Sponsors

HADOKS
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients 18 years and older who visit the corona urgent primary care facility of the HADOKS (location Haga, Leyweg, The Hague) or the SHR/DDDB (location Alrijne, Leiderdorp).

Exclusion criteria

Exclusion criteria: Children younger than 18 years of age. Insufficient understanding of the Dutch language. Recent (

Design outcomes

Primary

MeasureTime frame
Sensitivity, specificity, positive and negative predictive values of the Abbott PanBio antigen test in relation to the RT-PCR (reference test).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)