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Link Between Eosinopenia and Bacterial Infections in the Elderly Subject Hospitalized in Geriatrics (ELISA)

G

Gérond'if

Status

Completed

Conditions

Fever
Leukocytes
C Reactive Protein (CRP) is Less Than 20 mg/ l

Study type

Observational

Funder types

Other

Identifiers

NCT04363138
2020-A00301-38

Details and patient eligibility

About

The main purpose of this monocentric, non-interventional, prospective study carried out in acute geriatrics (UGA) and post-rehabilitation care, is to determine if eosinopenia is associated with bacterial infections.

Full description

It's a monocentric, non-interventional, prospective study carried.

At inclusion:

Non-opposition will be collected by the investigator upon entering the Geriatric Unit.

The investigators will have all the biological and radiological results and will decide whether or not to start antibiotic treatment.

Patients will be divided into 2 groups: group with bacterial infections and the other with non-bacterial diseases.

The patient's socio-demographic data, reason for hospitalization, history, BMI, state of dependence (ADL-IADL), MMSE, treatments will be collected. Biological examinations in the phase where an infection is not suspected will also be collected (NFS, ionogram, urea, creatinemia, albumin, pre albumin, CRP, hepatocellular workup. Clinical examination during the episode may be infectious as well that biological and radiological data will be collected as well as the diagnosis made.

Antibiotic treatment is prescribed will be listed. The blood levels of eosinophils between the two groups will be compared.

Follow-up at 1 month:

The effectiveness of antibiotics will be evaluated on the absence of inflammatory syndrome and fever after the recommended antibiotic treatment and the duration of the recommended treatment. Vital status will be collected.

Enrollment

156 patients

Sex

All

Ages

75+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalized in Geriatrics.
  • First episode of:
  • Fever> 38 ° motivating the realization of a biological assessment.
  • Or Leukocytes> 10 g / l and C reactive protein (CRP) > 20 mg / l.
  • Be affiliated to a social security scheme.
  • No oral opposition to participation in the study and use of the data.

Exclusion criteria

  • Immunosuppression (HIV with CD4 <200 / mm3)
  • Active corticosteroid therapy
  • Asthma
  • Chemotherapy, immunosuppressive treatment
  • Malignant hematological disease, lympho or myeloproliferative syndrome
  • Antibiotic therapy initiated before entering the geriatric ward
  • Documented parasitosis
  • Eosinophilic vasculitis
  • stroke <30 days
  • Patient already included in another study
  • Patient under guardianship or curatorship
  • Not affiliated with a social security scheme
  • Oral opposition to participation in the study

Trial design

156 participants in 2 patient groups

bacterial infection
Description:
Patients with bacterial infection
No bacterial infection
Description:
Patients without bacterial infection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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