Cerebrolycin for Treatment of Covid-related Anosmia and Ageusia
Covid19 Related Anosmia and Aguesia
About this trial
This is an interventional treatment trial for Covid19 Related Anosmia and Aguesia focused on measuring COVID-19, ; anosmia, ; ageusia, ; cerebrolysin
Eligibility Criteria
Inclusion Criteria:
- A random sample of at least 250 adults with sudden hyposmia/anosmia and/or hypoageusia/ageusia during COVID-19 pandemics and experienced persistent olfactory and/or gustatory manifestations after recovery from other acute viral manifestations.
- compliance for drug intervention (group 1) or olfactory training (group 2) for at least 8 weeks.
Exclusion Criteria:
- Prior neurologic, medical or psychiatric disease.
- Other known infection at onset
- Nasal congestion
- Nasal polyps
- Surgery or head trauma or radiation for head and neck cancers as may result in injury to the nerves that control smell
- Exposure to toxic chemicals (such as pesticides and solvents)
Sites / Locations
- Assiut University Hospitals, Faculty of Medicine
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Olfactory and gustatory disorders after covid 19 infection (n = 150)
control group (n = 100)
Cerebrolysin Dose:5 ml ampoule (1ml contains 215.2 mg cerebrolysin) once daily through intramuscular injection five times per week, for a total of 40 treatments (for at least 8 weeks after presentation), after which the cycle was repeated again according to the each patient response to therapy for a maximum of 24 weeks.
no drug intervention, just olfactory training using at least 4 strong odors to smell twice daily for at least 15 minutes (every time), for at least 8 weeks after presentation.