Actively Recruiting
Clinical Study on the Treatment of Rhinitis Sicca With Sodium Hyaluronate Adjustable Nasal Irrigator
Led by China-Japan Union Hospital · Updated on 2025-12-29
200
Participants Needed
1
Research Sites
51 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To observe the therapeutic effect of sodium hyaluronate adjustable nasal irrigator on various types of rhinitis sicca and compare it with the therapeutic effect of the commonly used physiological seawater nasal spray in clinical practice.
CONDITIONS
Official Title
Clinical Study on the Treatment of Rhinitis Sicca With Sodium Hyaluronate Adjustable Nasal Irrigator
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Symptoms: Dry nose sensation, little and thick nasal discharge, nosebleeds, itchy nasal cavity, and dryness in the nasopharynx. Physical signs: Nasal endoscopy often reveals dry and congested nasal mucosa, which appears grayish-white or dark red, losing its normal luster. There are often dry, thick secretions, scabs or blood scabs on it. The surface of the nasal mucosa is eroded and ulcers occur. The mucosal lesions are most obvious in the anterior part of the nasal cavity. A diagnosis can be made if one or more of the above symptoms and signs are present.
You will not qualify if you...
- Those with dry rhinitis and chronic inflammation of the lower respiratory tract.
- Those confirmed by examination to be caused by certain latent lesions in the mouth, nose, throat, esophagu.s, neck or the whole body
- Those who have used drugs for treating dry rhinitis or other medications within the past 30 days.
- Pregnant or lactating women.
- Those who are allergic to this medicine.
- Those with severe cardiovascular, liver, kidney and hematopoietic system diseases, etc.
- Mentally ill patients.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
China-Japan Union Hospital of Jilin University
Changchun, Jilin, China, 130000
Actively Recruiting
Research Team
C
Cuida Meng, Doctor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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