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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04002349
Other study ID # TR-Med-NAR-Cluster
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2019
Est. completion date March 31, 2020

Study information

Verified date June 2019
Source Beijing Tongren Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Chronic rhinitis (CR) is one of the most common nasal mucosal diseases in the world. In China, about 140 million people suffer from this disease. Chronic rhinitis can lead to severe economic and social burden, as well as the potential risk of developing other chronic diseases such as asthma and chronic sinusitis. Therefore, it is of great significance to explore the classification and treatment strategies of chronic rhinitis in order to improve the health level of Chinese people.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date March 31, 2020
Est. primary completion date December 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Not younger than 18 years old

- Diagnosed as idiopathic rhinitis

- Signed and volunteered for the study

Exclusion Criteria:

- Comorbid airway diseases including (but not limited to) upper airway infection, chronic rhinosinusitis, nasal polyps

- Allergic to the medicines about to study

- Having used oral glucocorticoids or antihistamine agents within 30 days of the enrollment

Study Design


Related Conditions & MeSH terms

  • Common Cold
  • Determination of the Efficacy of Different Medications for Idiopathic Rhinitis
  • Impact of Different Medications on Biomarkers of Idiopathic Rhinitis
  • Rhinitis
  • Safety and Tolerance of Different Medications for Idiopathic Rhinitis

Intervention

Drug:
Budesonide Nasal Spray (Rhinocort, Shanghai Johnson & Johnson Pharmaceuticals, Ltd.)
Detailed in arm descriptions
Levocabastine Nasal Spray (Livostine, Shanghai Johnson & Johnson Pharmaceuticals, Ltd.)
Detailed in arm descriptions
0.9% natural saline
Detailed in arm descriptions

Locations

Country Name City State
China Beijing Tongren Hospital Beijing Beijing
China Yifan Meng Beijing Beijing

Sponsors (3)

Lead Sponsor Collaborator
Beijing Tongren Hospital Beijing Institute of Otolaryngology, Shanghai Johnson & Johnson Pharmaceuticals, Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Relief of bothersome symptoms Determined by change of visual analog scale for symptoms 2 weeks