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Study identifier: NCT06829706 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The Efficacy of Modified Olfactory Training Method for Patients With Post-viral Olfactory Dysfunction

Condition: Olfactory Dysfunction · Post Viral Olfactory Dysfunction (PVOD)  ·  Sponsor: Peking University Third Hospital

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to validate the effectiveness of the modified olfactory training device, the main questions it aims to answer are: Is the modified olfactory training device effective in treating patients with post-viral olfactory dysfunction? Compared to the conventional device, how efficient is the modified olfactory training device for improving olfactory function?

This description comes directly from the study's public registry record.

Talk to the study team

Dawei Wu, MD, PhD  ·  13522503401  ·  davidwuorl@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

BejingBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06829706