Investigating Anosmia and Ageusia in COVID-19 Adult Patients in Saudi Arabia

Completed

• Conditions: Ageusia; Covid19; Anosmia; Corona Virus Infection
• Interventions: Other: NHANES smell and taste tests

• Registration Number: NCT04388618
• Lead Sponsor: Princess Nourah Bint Abdulrahman University

Brief Summary

COVID-19 has adversely affected the healthcare system across the world. The world was not prepared for global outbreak of infectious diseases. The rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is enabling researchers worldwide to acquire a large amount of clinical data regarding coronavirus disease (COVID-19).

The COVID-19 infection severely affects the respiratory system in the critical cases and results in mortalities. The affected people experience a dry cough, fever, breathing problems, diarrhea, muscle pain, and sore throat. Besides that, some of the evidence from Italy, South Korea, China, and Spain suggest that the COVID-19 cases also lose their senses of smell and taste resulting in alterations in those patients.

The objective of this proposed study is to determine whether COVID-19 cases have Olfactory and gustatory dysfunctions as a hallmark indicator and can be used as diagnostic tools for the isolation of suspected people.

Investigators are presenting a prospective proportional case-control study that is conducted to investigate the COVID-19 cases with anosmia and /or Ageusia in a university hospital in Riyadh, Saudi Arabia. The sample size of this case series would be 250 cases of suspected COVID-19 patients. The cases included in the study are analyzed prospectively to determine if the cases had a history of anosmia and /or Ageusia, and then tested for the alteration of these senses through a panel of standardized odors/taste strips. That is looked at statistically allowing us to confirm the proposed effectiveness of these tests as a diagnostic tool.

Detailed Description

Upon identification of the patient in the triage area the research assistant will start the study by introducing the concept for the patient and then taking consent. The patient will go through the regular flow of patients in the ED and after being asked to do the swabs the research assistant will start the process of the study by testing the smell by the NHANES cards then directly assess the taste by the NHANES strips and documents the results on the cards and ask the patient to take a photo with his mobile and send it with his name to the primary investigator via a mobile application and dedicated phone number. The research assistant is the same person who is going to take the nasopharyngeal swab for the COVID-19 test. The cards are going to be collected in the negative pressure room of the patients and then discarded in the same room. The investigators in the study are not aware of which patient is answering what blinded investigator

Taste exam measures in NHANES The NHANES chemosensory tests used regional and whole mouth taste intensities of bitter and salt tastants as measures of taste function, which were similar to those implemented in the NIH Toolbox norming study. These NHANES taste measures were selected based on their ability to capture genetic and environmentally mediated variation in taste and for their potential relevance to diet and health.

Smell function in NHANES was assessed with an 8-item, odor identification test (Pocket Smell Tests™, Sensonics, Inc., Haddon Heights, NJ). Of many available psychophysical measures of olfactory function, odor identification tests are the most widely used in epidemiological and clinical settings, as they are quick, relatively inexpensive, and easy to administer. The odor identification test corresponds well with odor threshold tasks as well as other suprathreshold olfactory measures (e.g., discrimination, odor intensity), and hence is considered to be a rapid and accurate method for detecting olfactory dysfunction.

Study Timeline

• Study First Submitted: 2020-05-13
• Study First Submitted QC: 2020-05-13
• Study First Posted: 2020-05-14
• Study Start: 2020-06-15
• Primary Completion: 2021-12-31
• Study Completion: 2021-12-31
• Status Verified: 2022-05
• Last Update Submitted: 2022-05-02
• Last Update Posted: 2022-05-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 250

Inclusion Criteria

1- Suspected cases of COVID -19 fulfilling the case definition of Saudi CDC 2- Adult patients

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Exclusion Criteria

1. The cases of children under the age of 12 years

2. Known patients with Kallmann's syndrome, CHARGE syndrome, Indifference to pain syndrome, ciliopathy disorders.

3. Known patient with congenital anomalies, absent smell sense, and absent taste sense.

4. Pregnant and lactating ladies

5. Patients with trigeminal nerve disease

6. Blind and deaf patients

7. Malingering.

8. Adults aged more than 65 years old.

9. Allergy to quinine products

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
covid19 positive patients	NHANES smell and taste tests	participants who present with signs and symptoms suspected for covid19 and swabbed/tested positive
covid19 negative patients	NHANES smell and taste tests	participants who present with signs and symptoms suspected for covid19 and swabbed/tested negative

Primary Outcome Measures

Name	Time	Method
correlation of anosmia and ageusia to covid19 positive patients	from 1/06/2020 to 31/12/2020	to how extent alteration of smell and taste senses is related to covid19 status

Secondary Outcome Measures

Name	Time	Method
objective assessment of severity of smell and taste senses alterations in covid19 patients	from 1/06/2020 to 31/12/2020	to determine the range of sense affection ranging from total loss to mild form

Trial Locations

Locations (2)

prince Mohammed bin Abdulaziz Hospital; 🇸🇦 Riyadh, Central, Saudi Arabia

Princess Nourah Bint Abdulrahman Univeristy; 🇸🇦 Riyadh, Central, Saudi Arabia