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Olfactory Training Effects On Post-Covid-19 Hyposmia

Olfactory Training Effects On Post-Covid-19 Hyposmia: Therapeutic Intervention Impacts In Otorhinolaryngology

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
REBEC
Registry ID
RBR-10wqyg2r
Enrollment
Unknown
Registered
2021-07-20
Start date
2021-03-04
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronavirus as a cause of diseases classified in other chapters

Interventions

Olfactory training twice a day with four aromas (rose, eugenol citronelal, eucaliptol) for 3 months plus placebo pills (starch) 300mg twice a day for 3 months. (Control group with 64 participants). Ol
E02.190.888.061

Sponsors

Hospital Universitário Professor Edgard Santos- Universidade Federal da Bahia
Lead Sponsor
Hospital Universitário Professor Edgard Santos- Universidade Federal da Bahia
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with post-COVID olfaction disorders for more than 3 months; aged between 18 and 65 years; with diagnostic documentation of COVID-19 through a positive test for SARS-CoV-2.

Exclusion criteria

Exclusion criteria: Traumatic brain injury; neurodegenerative and psychiatric illness; pregnancy; allergic rhinitis or other rhinosinusopathy; presence of smell disorder prior to COVID-19; use of topical or systemic corticosteroid therapy in the last 30 days; as well as current use of alpha-lipoic acid; omega 3; vitamin A; zinc or pentoxifylline will be excluded. Patients with a history of smell disorder less than 3 months and all those with previous treatment of the olfactory complaint will also be excluded.

Design outcomes

Primary

MeasureTime frame
Objective improvement in olfactory function of at least 1 point in the Connecticut olfactory test after 12 weeks of treatment.

Secondary

MeasureTime frame
Subjective improvement of olfactory function through visual analogue scale assessment after 4, 8 and 12 weeks of treatment; olfactory function recovery time; correlation of collected clinical data with olfactory prognosis.

Countries

Brazil

Contacts

Public ContactLorena Figueiredo
lorenapfigueiredo@gmail.com+5571992607038

Outcome results

None listed

Source: REBEC (via WHO ICTRP)