Evaluation of the Prevalence of Anti-infective Drug Compliance in Pediatric Patients Hospitalized at Nimes University Hospital After Return Home (PEDIAOBST)

Nowadays, resistance to anti-infectives has become a global public health problem and its increased prevalence threatens human health.

To date, few studies have focused on drug compliance in the paediatric population and it varies according to the pathology This drug adherence in the paediatric population is directly linked to outpatient care by the parents or the child's immediate family. In addition, there are no studies on adherence to antibiotics prescribed at the end of hospitalization in the paediatric population.

In this context, it seems urgent to seek an intervention capable of leading to responsible and appropriate use of antibiotics in order to improve efficiency in the drug management of acute paediatric infections.

This pilot study would characterize pediatric patients and determine the compliance rate in this population.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

75

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Nîmes, France, 30029
        • Chu Nimes

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 16 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The patients included in the study are patients under 16 years of age (< 16 years of age) admitted to full hospitalization in the paediatric units

Description

Inclusion Criteria:

  • The patient is under 16 years of age (< 16 years of age).
  • The patient is admitted to a full hospitalization in one of the 2 paediatric units of the University Hospital of Nîmes.
  • The patient is discharged with a prescription for anti-infectives to be taken at home, for a maximum of 30 days.
  • The patient and the holder of parental authority are available for a follow-up of 1 month after discharge from hospital.

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Rate of patients observing anti-infectives
Time Frame: 2018
2018

Secondary Outcome Measures

Outcome Measure
Time Frame
Rehospitalization rates / emergency visits related to worsening infection
Time Frame: 2018
2018

Other Outcome Measures

Outcome Measure
Time Frame
Rate of observing patients who have recovered their anti-infective treatment
Time Frame: 2018
2018
Rate of observing patients who have taken anti-infective treatment as prescribed
Time Frame: 2018
2018
Sociodemographic and clinical characteristics
Time Frame: 2018
2018
Overall success rate in the quiz on understanding anti-infectives
Time Frame: 2018
2018

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 6, 2018

Primary Completion (Actual)

May 4, 2018

Study Completion (Actual)

June 10, 2018

Study Registration Dates

First Submitted

July 1, 2019

First Submitted That Met QC Criteria

July 3, 2019

First Posted (Actual)

July 5, 2019

Study Record Updates

Last Update Posted (Actual)

August 7, 2019

Last Update Submitted That Met QC Criteria

August 5, 2019

Last Verified

June 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • Mobilité/2017/GLB

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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