Prevalence and Outcomes of Olfactory and Gustatory Dysfunctions in Patients With COVID-19

Sponsor
Ain Shams University (Other)
Overall Status
Unknown status
CT.gov ID
NCT04524754
Collaborator
(none)
218
1
4.7
46.7

Study Details

Study Description

Brief Summary

Prevalence and Outcomes of Olfactory and Gustatory Dysfunctions in Patients with COVID-19

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    AIM OF THE STUDY AND WORK PLAN COVID-19 Hospitalized patients with confirmed diagnosis of disease will

    1. undergo questionnaire for prevalence of Anosmia/dysgeusia

    2. linking the anosmia/dysgeusia to the degree of disease and treatment outcomes.

    3. looking to improvement in anosmia/dysgeusia and its timing,

    METHODOLOGY Ethical committee approval for the current study protocol will be obtained. Patients will be invited to participate and the informed consent will be signed.

    Subjects and Setting:

    The clinical data of 218 patients with laboratory-confirmed COVID-19 infection will be collected from Ain Shams University Hospitals. In addition, other patients, infected physicians and nurses may voluntarily enroll in the study. Comorbidities as diabetes mellitus or hypertension, and chronic treatment lines taken will be documented, and considered in the analysis of the data. Patients would be receiving the ASU treatment protocol for covid 19.

    The following inclusion criteria will be considered: adult (>18 year); laboratory-confirmed COVID-19 infection (reverse transcription polymerase chain reaction, RT-PCR). The following exclusion criteria will be considered: patients with olfactory or gustatory dysfunctions before the epidemic; patients without a laboratory-confirmed COVID-19 infection diagnosis; patients who were in the intensive care unit at the time of the study (due to their health status).

    Clinical Outcomes Clinical data will be collected during the ear, nose, and throat (ENT) consultation; in the patient's room.

    Questions about olfactory function; questions investigating gustatory function; and questions about the treatment of the COVID-19 infection. All patients will be asked to answer these questions.

    Olfactory and Gustatory Outcomes The occurrence of olfactory dysfunction has been identified through several questions including social, eating, annoyance, and anxiety questions. The rest of the olfactory and gustatory questions will be based on the smell and taste. The questions have been chosen to characterize the variation, timing and associated-symptoms of both olfactory and gustatory dysfunctions, and, therefore, they suggest a potential etiology. Also the mean recovery time of olfaction will be assessed through 4 defined propositions: 1-4 days; 5-8 days; 9-14 days and >15 days.

    Statistical Analysis First, the following descriptive analysis will be done: frequency, percentages, mean and standard deviation (SD). Thereafter, a comparison will be done using Student t-test for quantitative variables and Fisher exact test for qualitative variables.

    Statistical Package Data entry and statistical analysis will be done using Statistical Package for Social Science (SPSS) version 20.0.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    218 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Retrospective
    Official Title:
    Prevalence and Outcomes of Olfactory and Gustatory Dysfunctions in Patients With COVID-19
    Actual Study Start Date :
    Jul 11, 2020
    Anticipated Primary Completion Date :
    Sep 11, 2020
    Anticipated Study Completion Date :
    Nov 30, 2020

    Outcome Measures

    Primary Outcome Measures

    1. olfaction [one month]

      subjective on a scale from 1 to 5 ( 1 is the least and 5 is the best ) , the score will be recorded for olfaction before and after the olfactory loss

    Secondary Outcome Measures

    1. gustation [one month]

      subjective on a scale from 1 to 5 ( 1 is the least and 5 is the best ) , , the score will be recorded for gustation before and after the gustatory loss

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • adult (>18 year); laboratory-confirmed COVID-19 infection (reverse transcription polymerase chain reaction, RT-PCR).
    Exclusion Criteria:
    • patients with olfactory or gustatory dysfunctions before the epidemic; patients without a laboratory-confirmed COVID-19 infection diagnosis; patients who were in the intensive care unit at the time of the study (due to their health status).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ain shams Univesrity Cairo Egypt

    Sponsors and Collaborators

    • Ain Shams University

    Investigators

    • Study Director: ethical committee, Ain Shams University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Mohamed Shehata Taha, Professor Doctor, Ain Shams University
    ClinicalTrials.gov Identifier:
    NCT04524754
    Other Study ID Numbers:
    • FMASUP46a/2020
    First Posted:
    Aug 24, 2020
    Last Update Posted:
    Aug 28, 2020
    Last Verified:
    Aug 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 28, 2020