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Comparison of bilateral anterior ethmoidal neurectomy versus combined anterior ethmoidal and sphenopalatine neurectomy for moderate-severe persistent allergic rhinitis

Comparison of bilateral anterior ethmoidal neurectomy versus combined anterior ethmoidal and sphenopalatine neurectomy for moderate-severe persistent allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128355
Enrollment
Unknown
Registered
2026-07-17
Start date
2025-02-03
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Moderate-severe persistent allergic rhinitis

Interventions

Control group (bilateral anterior ethmoidal neurectomy group):Endoscopic bilateral anterior ethmoidal neurectomy
Intervention group (bilateral anterior ethmoidal + sphenopalatine neurectomy group):Endoscopic bilateral anterior ethmoidal + sphenopalatine neurectomy

Sponsors

First Affiliated Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years, with no gender limitation; 2. Diagnosed as moderate-severe persistent allergic rhinitis in accordance with the 2022 edition of the "Guidelines for the Diagnosis and Treatment of Allergic Rhinitis in China"; 3. Poor control of main symptoms, significantly affecting life after conservative treatment, and/or unable to adhere to long-term desensitization therapy; 4. Strong willingness to undergo surgery, understanding the content and purpose of the study, and signing the surgical consent form and the informed consent form for enrollment.

Exclusion criteria

Exclusion criteria: 1. With mental illness or poor compliance; 2. Poor general condition, unable to tolerate surgery; 3. Aged 70 years; 4. With bleeding tendency or coagulation dysfunction; 5. Without receiving conventional drug therapy or immunotherapy; 6. Uncontrolled asthma or in acute exacerbation; 7. Combined with nasal tumors detected by preoperative examination.

Design outcomes

Primary

MeasureTime frame
VAS nasal symptom score;RQLQ quality of life score;

Secondary

MeasureTime frame
Levels of substance P, NPY, periostin, IL-5 and eotaxin-2 in nasal lavage fluid;Nasal resistance and acoustic rhinometry parameters;Incidence of postoperative complications (headache, dry eye, palatal numbness, etc.);Pulmonary function;Nitric oxide;

Countries

China

Contacts

Public ContactWei Hongquan

First Affiliated Hospital of China Medical University

18041363094@163.com+86 139 4043 7387

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026