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Teatment to the allergic rhinitis with intronasal corticosteroids and its impact on the lower airway

Teatment to the allergic rhinitis with intronasal corticosteroids and its impact on the lower airway

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13004022
Enrollment
Unknown
Registered
2013-05-20
Start date
2012-11-30
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

allergic rhinitis

Interventions

allergic treatment group:Budisonide nasal spray and nasal irrigation
allergic control group:Placebo spray and nasal irrigation

Sponsors

Nanjing Jinling Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. adults age 18~65; 2. gender not limited; 3. the diagnosis of allergic rhinitis (the Chinese medical association, guide to diagnosis and treatment of allergic rhinitis 2009); 4. no history of asthma symptoms (wheezing, short of breath, chest tightness, cough) or diagnosis of asthma; 5. no immune and nasal surgery treatment in recent six months; 6. no oral, suction, injected hormone therapy among recent one month; 7. in recent one month, no respiratory tract infection, no abnormal anatomy of the nasal cavity, nasal polyps, nasal septum deviation, etc.); 8. no using theophylline and leukotriene antagonists now; 9. there is no history of smoking or in one year, and smoking < 7 bags/year; 10. the subjects must voluntarily participate in the study, and comply with the requirements of the study, understand and comply with the corresponding examination; 11. comply with the drug dosage and follow-up plan.

Exclusion criteria

Exclusion criteria: 1. with COPD, interstitial pneumonia, such as the other types of chronic respiratory system disease been diagnosed; 2. concomitant other system serious disease (e.g., cardiovascular, metabolism, immunity, neural, urinary and blood, etc.); 3. temperature more than 37.5 degree C, or abnormal blood sample (white blood cell count >10*10^9/L or <4*10^9/L); 4. history of drug abuse, alcohol abuse or anesthesia or with a history of mental illness and against personality, motivation, suspicious, or other emotional or mental issues that may affect participation in the study of knowledge effectiveness; 5. pregnancy, lactation women; 6. participating in clinical trial projects or other drugs in process, can't cooperate with related inspection or for other reasons can't collaborators.

Design outcomes

Primary

MeasureTime frame
Eosinophil in nasal lavage;Eosinophil in induced sputum;FeNO;branchial provocation test;Histamine nasal provocation test;Eosinophil count in blood;Total IgE in serum;Total IgE in serum;

Countries

China

Contacts

Public ContactWang Qiuping

Nanjing Jinling Hospital

qpwang1016@vip.sina.com+86 135850106071

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026