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Role of Eustachian tube surgery in the treatment of chronic secretory otitis media

Not Applicable
Conditions
Surgical intervention of chronic secretory otitis media
Ear, Nose and Throat
Registration Number
ISRCTN38272958
Lead Sponsor
The Sixth Medical Center of PLA General Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
480
Inclusion Criteria

1. Age 18 to 70 years (including borderline values), with no restriction on gender
2. Patients diagnosed with chronic secretory otitis media, with no restriction on side, and those who meet the criteria in both ears can be included.
3. History of chronic secretory otitis media greater than 3 months.
4. Complete tympanic membrane with clear middle ear effusion on otoscopic examination.
5. Conductive deafness.
6. Acoustic conduction resistance with type B or C curve.
7. Negative for Valsalva.
8. History of previous tympanic membrane puncture or medication (nasal spray hormone and/or mucus promoter, etc.).
9. Patients who are to be treated with tympanic tube placement or eustachian tube balloon dilation for the first time and meet the indications for the surgery.

Exclusion Criteria

1. Fluctuating sensorineural deafness.
2. Otoscopic examination of the tympanic membrane with adhesions to the tympanic capsule or the presence of otitis externa (oozing from the external ear canal, fungal infection, etc.)
3. Clear presence of abnormal opening of the eustachian tube or other eustachian tube diseases.
4. Eligible for surgical treatment due to other nasal, sinus or ear diseases.
5. History of surgery on the affected middle ear and nasal cavity or nasopharynx.
6. History of cleft palate or other deformities or related surgical repair.
7. History of head or neck surgery or radiation therapy
8. Patients with ciliary immobility syndrome.
9. Expected survival for malignancy <12 months.
10. Patients with other conditions that, in the opinion of the investigator, are not suitable for participation in this study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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