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To explore the role of Biprofen nasal spray, hormone spray and their combination in various types of rhinitis

To explore the role of Biprofen nasal spray, hormone spray and their combination in various types of rhinitis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058263
Enrollment
Unknown
Registered
2022-04-04
Start date
2022-04-06
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Rhinitis

Interventions

Control group:Normal saline
Group 1:Birofen
Group 2:Nasal hormone
Group 3:Birofen and nasal hormones

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-60 years; 2. Patients who meet any of the following criteria: (1) Patients diagnosed with CRSwNP according to the diagnostic criteria recommended in the European Position Paper on Sinusitis and nasal polyps, or double-positive ECP-MPO nasal discharge strips; (2) Patients with allergic rhinitis (according to ARIA criteria), skin prick test or serum specific IgE level 3 or above, or ECP-MPO nasal discharge strip ECP-positive; (3) Patients who meet the diagnosis of vasomotor rhinitis and the ECP-MPO nasal discharge test paper is completely negative; (4) Patients who meet the diagnosis of simple rhinitis and the ECP-MPO nasal discharge test paper is completely negative; 3. The patient agrees to participate in the experiment and signs the informed consent; 4. Patients judged by the investigator to meet the requirements of the protocol.

Exclusion criteria

Exclusion criteria: 1. Patients with nasal mucosa erosion, nasal mucosa ulcer and nasal septum perforation were found through nasal examination; 2. Patients receiving anticoagulant drugs within 5 days; 3. Nasal surgery within a month; 4. Patients with other nasal diseases that may lead to drug deposition in the nasal cavity, such as sinusitis, drug-induced rhinitis, nasal polyps or nasal structural abnormalities; 5. Patients with non-allergic rhinitis (vasomotor rhinitis, eosinophilic rhinitis); 6. Patients who received nasal surgery within 90 days before the start of the observation period were screened; 7. Patients with contraindications to desensitization; 8. Patients with recurrent nasal bleeding; 9. Patients suffering from complications such as severe liver disease, kidney disease, heart disease or blood disease; 10. The presence of alcohol or drug abuse/addiction may affect the progress of the study. Binge drinking is defined as having more than 14 units of alcohol per week (1 unit of alcohol =360 mL beer, 45 mL spirits at 40% alcohol or 150mL wine); 11. Systemic or topical use of antibiotics, intranasal hormones, intranasal or oral antihistamines within 1 week prior to sampling, systemic use of corticosteroids or immunosuppressants 3 weeks prior to sampling; 12. Upper respiratory tract infection or other acute infection within 30 days; 13. Patients judged by the investigator to be unsuitable subjects for this study.

Design outcomes

Primary

MeasureTime frame
Symptom score;

Countries

China

Contacts

Public ContactDeng Yuqin
qingerdeng0713@163.com+86 15972054520

Outcome results

None listed

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