drugset / Trial / NCT04853836

Summary

Olfactory dysfunction is common among patients with Corona-Virus-Infection-Disease (COVID)-19, and up to 30% of patients may report persistent disorders of smell or taste as a long-term sequelae. This randomized-controlled study has addressed to compare the efficacy of neuro-protective and anti-inflammatory agents palmitoylethanolamide (PEA) and Luteolin(Treatment) with control (olfactory training) in a cohort of patients who present persistent smell disorders after resolution from Covid-19 and negative swab for 4 months at least.

Timeline

Start
2020-11-15
Primary completion
2021-10-28
Completion
2022-08-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Luteolin Small molecule 70 mg Oral
Subject Luteolin Small molecule 140 mg Oral
Subject Palmidrol Small molecule 700 mg Oral
Subject Palmidrol Small molecule 1400 mg Oral

Indications