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Impact of Pharmaceutical Interviews Regarding the Management of Adverse Effects Related to the Antibiotic Therapy Used to Treat Osteoarticular Infections During Return Home

Impact of Pharmaceutical Interviews Regarding the Management of Adverse Effects Related to the Antibiotic Therapy Used to Treat Osteoarticular Infections During Return Home

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05248490
Acronym
EFIRAD
Enrollment
90
Registered
2022-02-21
Start date
2022-03-22
Completion date
2024-06-14
Last updated
2024-12-04

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

Conditions

Bone and Joint Infection

Keywords

osteo articular infection, adverse event, antibiotic treatment, pharmaceutical interview

Brief summary

The primary objective is to evaluate the impact of Pharmaceutical Interviews in the patient self-management of non-severe side effects caused by antibiotics prescribed for the treatment of osteoarticular infections when the patient returns home.

Interventions

Pharmaceutical interview with pharmacist: to be informed treatment taken and related SAE informations at the end of hospitalization

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Patient \> or =18 years; * Informed consent signed; * French-speaking and reading; * Affiliated to a social insurance; * Benefiting from medical and surgical care for an osteoarticular infection; * Treated with an oral antibiotic therapy on discharge from hospital. * Indication of the antibiotic therapy osteoarticular infection; * Return home immediately after discharge.

Exclusion criteria

* Refusal to participate * Protected adult patient, under guardianship or curatorship. * Minor patient * Patient benefiting from an AME. * Pregnant or breastfeeding woman. * Non-French speaking patient. * Patient unable to understand the course of the study. * Patient with a documented history of cognitive or psychiatric disorders. * Patient treated with oral antibiotic therapy for an indication other than osteoarticular infection. * Patient treated with parenteral antibiotic therapy. * Discharge: Institution (EHPAD), rehabilitation or other health establishment. * Patient systematically using one of the symptomatic treatments proposed in the discharge prescription before hospitalization.

Design outcomes

Primary

MeasureTime frameDescription
Adverse effects self-management measurementat day 7Phone call to evaluate the self-management of adverse effects. Self-management evaluation (optimal choice/non-optimal choice) performs thanks to the use of a standardized decision-tree. Proportion of patients with an optimal or non-optimal self-management.

Secondary

MeasureTime frameDescription
Patient knowledge assessmentat day 7Questionnaire, 12 points: * proportion of patients reaching a score upper than 10 * proportion of patients reaching a score between 6 and 9 * proportion of patients reaching a score lower than 6

Countries

France

Outcome results

None listed

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