Skip to content

Multicenter study of subcutaneous immunotherapy for obstructive sleep apnea with allergic rhinitis

Multicenter study of subcutaneous immunotherapy for obstructive sleep apnea with allergic rhinitis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101450
Enrollment
Unknown
Registered
2025-04-25
Start date
2025-04-25
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

obstructive sleep apnea, allergic rhinitis

Interventions

Control group:Conventional drug therapy
Experimental group:Subcutaneous immunotherapy

Sponsors

Shenzhen University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the diagnostic criteria for obstructive sleep apnea-hypopnea syndrome as stipulated in the "Chinese Guidelines for the Diagnosis and Treatment of Obstructive Sleep Apnea in Children (2020)" or the "Multidisciplinary Guidelines for the Diagnosis and Treatment of Obstructive Sleep Apnea in Adults"; 2. Meeting the diagnostic criteria for allergic rhinitis as outlined in the "Chinese Guidelines for the Diagnosis and Treatment of Allergic Rhinitis (2022, Revised Edition)", and confirmed to be caused by Dermatophagoides farinae and/or Dermatophagoides pteronyssinus (sIgE >= 0.35 IUA/L for Dermatophagoides farinae and/or Dermatophagoides pteronyssinus); 3. Age ranging from 5 to 65 years old; 4. Having received standardized anti-allergy conventional drug treatment for at least one year before enrollment; 5. Signing the informed consent form for the clinical trial.

Exclusion criteria

Exclusion criteria: 1. Patients whose legal guardians or themselves are unable to understand or comply with the research protocol; 2. Patients with severe psychological disorders or mental illnesses; 3. Patients with severe autoimmune diseases or immunodeficiency diseases; 4. Patients with malignant tumors; 5. Pregnant women; 6. Patients with contraindications to SCIT or at high risk of severe adverse reactions. 7. Patients who have undergone or are about to undergo OSA surgery; 8. Patients who have received or are about to receive biologics (such as omalizumab, Dupilumab); 9. Patients with moderate to severe atopic dermatitis.

Design outcomes

Primary

MeasureTime frame
Sleep respiratory monitoring;

Secondary

MeasureTime frame
Visual Analogue Scale;combined symptom and medication score;Nasal resistance;

Countries

China

Contacts

Public ContactLiming Li

Shenzhen University General Hospital

liliming1972@163.com+86 755 2183 9069

Outcome results

None listed

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