Prevalence and Outcomes of Olfactory and Gustatory Dysfunctions in Patients With COVID-19
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ClinicalTrials.gov Identifier: NCT04524754 |
Recruitment Status : Unknown
Verified August 2020 by Mohamed Shehata Taha, Ain Shams University.
Recruitment status was: Recruiting
First Posted : August 24, 2020
Last Update Posted : August 28, 2020
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Condition or disease |
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Anosmia |
AIM OF THE STUDY AND WORK PLAN COVID-19 Hospitalized patients with confirmed diagnosis of disease will
- undergo questionnaire for prevalence of Anosmia/dysgeusia
- linking the anosmia/dysgeusia to the degree of disease and treatment outcomes.
- 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 Type : | Observational |
Estimated 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 : | July 11, 2020 |
Estimated Primary Completion Date : | September 11, 2020 |
Estimated Study Completion Date : | November 30, 2020 |

- olfaction [ Time Frame: 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
- gustation [ Time Frame: 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

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Sampling Method: | Non-Probability Sample |
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).

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): NCT04524754
Contact: Fatma S Ebeid, MD | +20109556 9596 | dr.fatma_ebeid@yahoo.com |
Egypt | |
Ain shams Univesrity | Recruiting |
Cairo, Egypt | |
Contact: Fatma S Ebeid, MD +20109556 9596 dr.fatma_ebeid@yahoo.com |
Study Director: | ethical committee | Ain Shams University |
Publications:
Responsible Party: | Mohamed Shehata Taha, Professor Doctor, Ain Shams University |
ClinicalTrials.gov Identifier: | NCT04524754 |
Other Study ID Numbers: |
FMASUP46a/2020 |
First Posted: | August 24, 2020 Key Record Dates |
Last Update Posted: | August 28, 2020 |
Last Verified: | August 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Anosmia Olfaction Disorders Sensation Disorders Neurologic Manifestations Nervous System Diseases |