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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04484493
Other study ID # RC 4-7-2020
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date August 8, 2020
Est. completion date November 3, 2020

Study information

Verified date November 2020
Source Benha University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date November 3, 2020
Est. primary completion date October 25, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
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.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
mometasone furoate nasal spray
dose of 2 puff in each nostril (100 µg once daily each nostril).

Locations

Country Name City State
Egypt Benha University Hospital, Faculty of Medicine Banha Qalubia

Sponsors (1)

Lead Sponsor Collaborator
Benha University

Country where clinical trial is conducted

Egypt, 

References & Publications (2)

Heilmann S, Just T, Göktas O, Hauswald B, Hüttenbrink KB, Hummel T. [Effects of systemic or topical administration of corticosteroids and vitamin B in patients with olfactory loss]. Laryngorhinootologie. 2004 Nov;83(11):729-34. German. — View Citation

Hura N, Xie DX, Choby GW, Schlosser RJ, Orlov CP, Seal SM, Rowan NR. Treatment of post-viral olfactory dysfunction: an evidence-based review with recommendations. Int Forum Allergy Rhinol. 2020 Sep;10(9):1065-1086. doi: 10.1002/alr.22624. Epub 2020 Jun 25. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary improvement of olfaction 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). 3 weeks
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