Anosmia, Covid19
Conditions
Keywords
covid19, anosmia, mometasone nasal spray
Brief summary
The aim of this study is to evaluate the role of the topical corticosteroids nasal spray (mometasone furoate nasal spray) in improving anosmia in patients recovered from COVID-19 infection.
Detailed description
This study willbe submitted on patients who recently recovered from proven COVID-19 infection and complaining of anosmia or hyposmia.The proven COVID-19 infection will be relied on a positive real-time reverse transcription polymerase chain reaction (rRT-PCR) with samples obtained by a nasopharyngeal swab. The recovery is defined as 2 consecutives negative (rRT-PCR) samples. Complete medical history will be taken, and essential clinical assessment with appropriate protective measures will be performed in all patients.The patients in the study will be randomly divided into two groups: - Group I: -who will receive topical corticosteroid nasal spray (mometasone furoate nasal spray) beside olfactory training Group II: -who will not receive topical corticosteroid nasal spray but only olfactory training. As regards the assessment of smell,the patient will assess his smell sensation using familiar substances with distinctive odor. A jar of coffee, a branch of mint and garlic are some used substances. The patient will report the degree of anosmia subjectively with score on a scale from 0 to 10.The assessment of smell will be done initially after recovery/discharge, after 1 week, 2 weeks and after 3 weeks for all patients. The duration of smell loss will be recorded from the onset of anosmia till full recovery of the sensation.
Interventions
dose of 2 puff in each nostril (100 µg once daily each nostril).
Sponsors
Study design
Eligibility
Inclusion criteria
* adults 18 yrs or older patients * confirmed case (+ve PCR), * recovered/discharged (2 -ve PCR), * suffered from sudden recent anosmia or hyposmia
Exclusion criteria
* patients already on nasal steroid * with previous chronic rhinological pathologies, * patients on systemic steroid for previous systemic disease, * anosmia improved before COVID19 recovery, * pregnancy * patients who will not complete the follow up period.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| improvement of olfaction | 3 weeks | The patient will report the degree of anosmia subjectively with score on a scale from 0 to 10 (0 means total loss of smell and 10 refers to completely normal smell sensation). |
Countries
Egypt