Skip to content

Research on the mutual influence and mechanism between obstructive sleep apnea-hypopnea syndrome and the diagnosis and treatment of allergic rhinitis

Research on the mutual influence and mechanism between obstructive sleep apnea-hypopnea syndrome and the diagnosis and treatment of allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110082
Enrollment
Unknown
Registered
2025-09-30
Start date
2025-09-30
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Obstructive sleep apnea-hypopnea syndrome and allergic rhinitis

Interventions

Experimental group,:None
Control Group:None

Sponsors

Baoding NO.1 central hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The diagnosis of OSAHS complies with the standards of the "Diagnosis and Treatment Guidelines for OSAHS in Chinese Adults" and the "Diagnosis and Treatment Guidelines for Obstructive Sleep Apnea in Chinese Children (2020)". 2. The AR diagnosis complies with the standards of the "Guidelines for the Diagnosis and Treatment of Allergic Rhinitis" . 3. Age and basic condition: Aged between 5 and 70 years old, without having undergone nasopharyngeal surgery or systemic treatment for OSAHS/AR (such as CPAP, immunotherapy); 4. Voluntarily sign the informed consent form and commit to completing the 12-month follow-up and testing.

Exclusion criteria

Exclusion criteria: 1. Age mismatch; 2. Other nasal diseases, such as chronic sinusitis with nasal polyps (EPOS 2020 standard), nasal tumors, history of nasal trauma, and other diseases that may interfere with the assessment; 3. Systemic disease interference, such as severe cardiopulmonary diseases (NYHA cardiac function grade III-IV, COPD GOLD grade 3-4), immunodeficiency diseases (such as HIV/AIDS), and uncontrolled diabetes (HbA1c>=9%); 4. Drug or treatment interference, such as the use of immunosuppressants or biological agents (such as omalizumab) within the last 3 months; 5. Pregnant or lactating women; 6. Insufficient compliance, such as inability to cooperate with follow-up visits (such as living in a different place, mental illness) or refusal to undergo certain tests (such as repeated PSG or blood tests).

Design outcomes

Primary

MeasureTime frame
Reduce or increase;

Secondary

MeasureTime frame
Score.;Sleep apnea monitoring;

Countries

China

Contacts

Public ContactZhaoWei

Baoding NO.1 central hospital

doczhaowei@163.com+86 312 5976916

Outcome results

None listed

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