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Application and demonstration of using the sandwich method of repairing the eardrum during endoscopic

Application and demonstration of using the sandwich method of repairing the eardrum during endoscopic - Application and demonstration of using the sandwich method of repairing the eardrum during endoscopic

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082282
Enrollment
Unknown
Registered
2024-03-26
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

otitis media

Interventions

observation group:Using the sandwich method of repairing the eardrum during endoscopic

Sponsors

People's Hospital of Anshun city Guizhou Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Age 18-65 years old, gender is not limited; 2) Chronic otitis media or trauma caused by tympanic membrane perforation and more than 3 months do not heal; 3) The perforation of the tympanic membrane is located in the tense part, and there are central perforations of the residual tympanic membrane around the perforation; 4) First operation on the ear; 5) Electrical audiometry results suggest conductive or mixed hearing loss; 6) There is no tympanic inflammation or inflammation control, and no squamous epithelial invasion in the tympanic chamber; 7) The upper tympanum, tympanic sinus and mastoid were free of granulations, cholesteroma and other abnormalities; 8) Mucosal inflammation in tympanic and mastoid air chamber systems was in a resting state; 9) CT of temporal bone indicates that the auditory chain in the tympanic chamber is intact; 10) No serious systemic diseases, such as cardiovascular and cerebrovascular diseases, liver and kidney insufficiency, hematopoietic system diseases; 11) Subjects who are able to understand and abide by the study procedures and voluntarily participate in the study by signing the informed consent form (the informed consent is signed by themselves or their legal representatives).

Exclusion criteria

Exclusion criteria: (1) Relative contraindications: 1) cardiopulmonary insufficiency; 2) People with coagulation disorders; 3) middle ear cholesteatoma, suppurative otitis media acute stage; 4) Patients with small operating space and visual field in endoscopic surgery. (2) Absolute contraindications: 1) Patients with severe cardiopulmonary diseases, such as severe arrhythmia, acute stage of myocardial infarction, severe heart failure, asthma attack, respiratory failure and so on. 2) Suspected shock, gastrointestinal perforation and other critical patients. 3) Severe mental disorders and uncooperative mental patients. 4) Complicated with intracranial and extracranial complications of chronic suppurative otitis media, cholesteatoma of the middle ear, tympanosclerosis (types ?, ?, ?); 5) middle ear adhesions; 6) Combined with external, middle and inner ear deformity; 7) Patients with systemic diseases who cannot tolerate general anesthesia; 8) Combined with mental illness.

Design outcomes

Primary

MeasureTime frame
time of operation;Tympanic membrane recovery;Hearing recovery;Tympanic curve recovery;

Countries

China

Contacts

Public ContactYouxing Lan

People's Hospital of Anshun city Guizhou Province

lyxassymyy2022@163.com+86 135 9536 1911

Outcome results

None listed

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