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

Recruiting N/A Interventional Study
Olfactory Dysfunction Post Viral Olfactory Dysfunction (PVOD)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 80
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Peking University Third Hospital · Other
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About This Trial

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?

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age 18-80 years old, gender not limited. 2. Patients diagnosed with olfactory dysfunction following infections of the upper respiratory tract, as determined by Sniffin' Sticks test (including TDI value test). 3. Voluntarily signs the informed consent form. Exclusion Criteria…
Contacts

Dawei Wu, MD, PhD

13522503401

davidwuorl@163.com

CONTACT