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Perception of Smell and Taste During Antibiotic Treatment (OGUSTA)

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ClinicalTrials.gov Identifier: NCT03893279
Recruitment Status : Not yet recruiting
First Posted : March 28, 2019
Last Update Posted : March 29, 2019
Sponsor:
Information provided by (Responsible Party):
Hospices Civils de Lyon

Brief Summary:

Antibiotic use may be associated with effects on the perception of smell and taste. These effects are poorly known. The mechanisms can be very diverse, and the effect can be very variable depending on the type of antibiotic used, the dose, and the duration.

The aim of this study is to analyze the perception of the taste and olfactory capacities of patients, during an antibiotic treatment.


Condition or disease Intervention/treatment
Infectious Disease Behavioral: Smell and Taste and questionnaire

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Study Type : Observational
Estimated Enrollment : 30 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Perception of Smell and Taste During Antibiotic Treatment
Estimated Study Start Date : April 2019
Estimated Primary Completion Date : December 2021
Estimated Study Completion Date : January 2022

Resource links provided by the National Library of Medicine



Intervention Details:
  • Behavioral: Smell and Taste and questionnaire
    The questionnaire must be completed before the antibiotic is taken, if a change of antibiotic is planned (stop of a treatment or addition of another treatment) and at the end of the antibiotic treatment.


Primary Outcome Measures :
  1. Questionnaire on Perception of taste [ Time Frame: Time of antibiotic treatment (maximum 6 months) ]

    Collection of scores on perception of taste, during questionnaires to be completed before, during, and after taking antibiotics.

    Qualitative analysis.


  2. Questionnaire on Perception of smell [ Time Frame: Time of antibiotic treatment (maximum 6 months) ]

    Collection of scores on perception of smell, during questionnaires to be completed before, during, and after taking antibiotics.

    Qualitative analysis.




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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patient meeting the eligibility criteria followed in the department of Infectious and Tropical Diseases of the Croix Rousse Hospital of the Civil Hospitals of Lyon
Criteria

Inclusion Criteria:

  • Major patient
  • Patient with bacterial infectious disease requiring antibiotic treatment.
  • Having been informed about the study and not having opposed to participate

Exclusion Criteria:

  • Patient under legal protection
  • Patient refusing to participate

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03893279


Contacts
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Contact: Tristan FERRY, Pr 04 72 07 24 81 ext +33 tristan.ferry@chu-lyon.fr

Locations
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France
Department of Infectious and Tropical Diseases of the Croix Rousse Hospital of the Civil Hospitals of Lyon Not yet recruiting
Lyon, France, 69004
Contact: Tristan FERRY, Pr    04 72 07 24 81 ext +33    tristan.ferry@chu-lyon.fr   
Principal Investigator: Tristan FERRY, Pr         
Sponsors and Collaborators
Hospices Civils de Lyon

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Responsible Party: Hospices Civils de Lyon
ClinicalTrials.gov Identifier: NCT03893279     History of Changes
Other Study ID Numbers: 69HCL19_0117
First Posted: March 28, 2019    Key Record Dates
Last Update Posted: March 29, 2019
Last Verified: March 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Communicable Diseases
Infection
Anti-Bacterial Agents
Antibiotics, Antitubercular
Anti-Infective Agents
Antitubercular Agents