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Assessment of the Effectiveness and Safety of Posterior Nasal Nerve Combined with Anterior Ethmoid Neurotomy in Patients with Idiopathic Rhinitis: a Multicentre, Randomised, Parallel-controlled Study
The present study was a randomised, parallel controlled, open-label, multicentre clinical study. The trial was divided into two groups, the posterior nasal nerve combined with anterior ethmoid neurotomy group (group A) and the conventional drug treatment group (group B). Patients with idiopathic rhinitis (IR) who met the inclusion criteria were included in a 7-day introductory period of nasal spray hormone (Budesonide nasal spray) treatment. Subjects with IR who met the randomization criteria after the introductory period were randomized 1:1 to either group A or group B for a 1-year treatment follow-up study. In group A, subjects will undergo the posterior nasal nerve combined with anterior ethmoid neurotomy. In group B, subjects will be treated with medication according to guideline recommendations when nasal-related symptoms occur. Oral antihistamines (Loratadine) or nasal antihistamines (Azelastine Hydrochloride) are preferred, and nasal hormones (Budesonide nasal spray), or a combination of two or three drugs, may be used in severe cases. Participants will be evaluated for safety and efficacy throughout the entire three-year period.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Renmin Hospital of Wuhan University
Wuhan, Hubei, China
Renmin Hospital of Wuhan University
Wuhan, Hubei, China
Start Date
March 1, 2025
Primary Completion Date
December 30, 2025
Completion Date
December 30, 2026
Last Updated
March 11, 2025
150
ESTIMATED participants
Posterior nasal nerve combined with anterior ethmoid neurotomy
PROCEDURE
Drug therapy group
DRUG
Lead Sponsor
Xu Yu
Data Source & Attribution
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