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Impact of the Use of CRP on the Prescription of Antibiotics in General Practitioners

Impact of the Use of C-reactive Protein in a Micro-method on the Prescription of Antibiotics in General Practitioners Consulting in the Office

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03540706
Acronym
VIP
Enrollment
406
Registered
2018-05-30
Start date
2018-05-01
Completion date
2023-03-13
Last updated
2023-08-07

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

Conditions

Respiratory Infection, Respiratory Infections in Children

Keywords

Respiratory Infections, C-reactive protein, antibiotic prescription

Brief summary

Respiratory infections, including episodes of coughing with fever, are the main cause of outpatient antibiotic prescription, while a minority of them are linked to bacterial infections requiring antibiotic. These prescriptions are often performed by general practitioners. These unnecessary antibiotic contribute to increased bacterial resistance, side effects and unnecessary costs. Campaigns for the correct prescription of antibiotics have had a real but partial or transient success. C-reactive protein micro-method (POCT-CRP) could help to differentiate between viral and bacterial infections and thus contribute to the proper use of antibiotics. The decrease in prescription of antibiotics is likely to have an even stronger positive impact in countries like France, where prescription is high. The objective of this study is to evaluate the use of POCT-CRP in the general practitioner's office in case of suspected respiratory infection.

Interventions

DIAGNOSTIC_TESTCare with C-reactive protein assay in micro method

Care with C-reactive protein assay in micro method

Sponsors

Association Clinique Thérapeutique Infantile du val de Marne
CollaboratorOTHER
Centre Hospitalier Intercommunal Creteil
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* Age ≥ 3 years * Clinical suspicion of respiratory infection defined by the presence of at least one respiratory sign among, cough, dyspnea, chest pain and auscultatory abnormality and at least one general sign among fever, sweat, headache, myalgia, impairment of general condition * Affiliated to a social health insurance * Signed consent

Exclusion criteria

* Duration of symptoms \< 24 hours * Hospitalization or emergency assessment decision decided from the outset * Signs of severity before the realization of POCT-CRP * Patient previously included in the study for the same episode * Antibiotic therapy within 7 days * Chronic cough (more than 3 weeks)

Design outcomes

Primary

MeasureTime frameDescription
Frequency of antibiotic therapy prescribed10 dayswith and without POCT-CRP

Secondary

MeasureTime frameDescription
Frequency of antibiotic therapy prescribed in patients aged from 3 to 17 years old10 dayswith and without POCT-CRP
Frequency of antibiotic therapy prescribed in patients older than 65 years old10 dayswith and without POCT-CRP
Type of antibiotic prescribed10 days
Frequency of complementary exam10 dayswith and without POCT-CRP
type of complementary exam10 dayswith and without POCT-CRP
Frequency of antibiotic therapy prescribed in patients aged from 18 to 64 years old10 dayswith and without POCT-CRP
Proportion of number of patients with delayed antibiotic therapy10 dayswith and without POCT-CRP
number of prescription following the recommended algorythms10 daysAdequacy between the proposed decision algorithm according to the C-reactive protein assay and the antibiotic prescription
Concordance between the prescription proposed by the decision algorithm as a function of the micro-CRP and the prescription realized: kappa coefficient10 daysThe assessment of the utility of the POCT procedure
COVID-19 positive patients1 dayNumber of COVID-19 positive patients by diagnostic method (From October 2020)
Proportion of number of patients referred to emergency10 dayswith and without POCT-CRP

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026