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A comparative study on rush immunotherapy of allergic rhinitis combined with omazumab.

A comparative study on rush immunotherapy of allergic rhinitis combined with omazumab.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035507
Enrollment
Unknown
Registered
2020-08-13
Start date
2021-06-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

allergic rhinitis

Interventions

control group:common specific immunotherapy
experimental group:rush immunotherapy

Sponsors

Tongji Hospital of Tongji University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Subjects shall be Chinese citizens aged 18 to 60 years; 2. Subjects must be diagnosed with AR during screening and baseline follow-up, and allergen test results are positive for dust mites.Subjects must be diagnosed with AR during screening and baseline follow-up, and allergen test results are positive for dust mites; Diagnostic criteria for AR: At least 3 of the 4 symptoms of nasal itching, sneezing, runny nose and nasal congestion, with a score of 2 or more for at least 2 of the symptoms. Chinese journal of otorhinolaryngology head and neck surgery, 2016,51 (01):6-24). 3. The subject is in good health and has no clinically significant disease that interferes with the test schedule or operation or affects the safety of the subject; 4. Subjects shall be able to comply with the treatment and follow-up schedule; 5. Fertile female subjects must have negative urine HCG at screening.

Exclusion criteria

Exclusion criteria: 1. Subjects with acute sinusitis and acute nasal infection; 2. Subjects with any clinical abnormalities in vital signs or clinically significant abnormalities in ecg results at screening or baseline follow-up; 3. Subjects with clinically significant cardiovascular, lung, kidney, liver, metabolic disease, hematological or neurological disease, or subjects with impaired immune system; 4. Subjects suffering from upper respiratory tract infection; 5. Subjects with septal deviation requiring corrective surgery; 6. Subjects are members of the research team directly involved in this study; 7. Subjects with nasal vestibular inflammation, nasal tumor and other nasal diseases; 8. Subjects plan to get pregnant within three months; 9. Subjects who have participated in clinical drug trials within three months; 10. Subjects who used drugs that may affect the results of the test and stop for less than the prescribed time.

Design outcomes

Secondary

MeasureTime frame
The concentration of NO in nasal exhalation;

Primary

MeasureTime frame
symptom and sign score of allergic rhinitis;

Countries

China

Contacts

Public ContactYu Shaoqing

Tongji Hospital of Tongji University

yu_shaoqing@163.com+86 13916455012

Outcome results

None listed

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