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Effect analysis of sublingual desensitization on inner ear function in patients with allergic rhinitis

Effect analysis of sublingual desensitization on inner ear function in patients with allergic rhinitis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114928
Enrollment
Unknown
Registered
2025-12-19
Start date
2025-11-19
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Allergic rhinitis

Interventions

Blank group:None
Control group:None
Observation Group:None

Sponsors

Meishan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged between 14 and 60 years; 2. Willing to pay for dynamic testing of serum-specific sIgE and total IgE to evaluate treatment effectiveness and future treatment value, and able to cooperate with clinical nasal examinations, SPT, audiological tests, and rating scales at each mid-term research visit; 3. Medical history shows no hearing loss, no history of noise exposure, no history of ototoxic drug use, no metabolic disorders, and no neurological problems; 4. Audiology and otoscopic examinations show normal cochlear and middle ear function. Participants with double mite positive results of 2 or higher on SPT or positive dust mite-specific IgE will be enrolled in the observation group; if SPT or serum-specific IgE results are negative, they will be enrolled in the blank group; 5. The patient or the patient’s family must fully understand the AR treatment plan, have a thorough understanding of the SLIT process, possible risks, and contraindications, and voluntarily choose SLIT; 6. Patients who can adhere to SLIT and maintain regular follow-up.

Exclusion criteria

Exclusion criteria: 1. Age under 14 or over 60; 2. Patients with a history of external ear trauma, use of ototoxic drugs, any systemic or metabolic disorders leading to hearing loss, tympanic membrane perforation, other middle ear pathologies, or previous ear surgeries; 3. Inability to cooperate with clinical nasal local examination, SPT, audiological tests, or rating scales; 4. SLIT patients who drop out midway or are unable to cooperate with follow-up should be excluded; 5. Those who refuse to participate in this study.

Design outcomes

Primary

MeasureTime frame
Audiology tests (average hearing threshold, tympanometry, otoacoustic emission signal-to-noise ratio, acoustic reflex threshold, ABR);

Secondary

MeasureTime frame
Skin Prick Test (SPT) Results;Serum-specific sIgE (against house dust mites/dust mites);

Countries

China

Contacts

Public ContactLiu Danfeng

Meishan People's Hospital

290361202@qq.com+86 18123037211

Outcome results

None listed

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