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A prospective study on the treatment of patients with sudden deafness and diabetes with two different ways of administration

A prospective study on the treatment of patients with sudden deafness and diabetes with two different ways of administration

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015954
Enrollment
Unknown
Registered
2018-05-02
Start date
2018-03-01
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Sudden hearing loss

Interventions

Experimental group:intratympanic injection glucocorticoid
Control group:systemic glucocorticoid

Sponsors

Peking Unversity Shenzhen hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years old; 2. A sudden onset of sensorineural hearing loss within 72 hours, at least in the three consecutive frequency of hearing loss of >=30dBHL; 3. Unilateral onset; 4. Confirmed diabetes; 5. The time of onset is within 30 days. 6.The hearing loss must have been deemed idiopathic following a suitable otolaryngologic evaluation, including medical and otologic history and extensive systems review, head and neck and otologic and neurotologic physical examination, audiometry, and imaging to rule-out structural or retrocochlear pathology, such as vestibular schwannoma, stroke, or demyelinating disease.

Exclusion criteria

Exclusion criteria: 1. External ear inflammation, tympanitis, or external auditory canal swelling in the ears; 2. The affected ear diagnosed with Meniere's disease, chronic suppurative otitis media or cholesteatoma of the middle ear, ear sclerosis; 3. History of congenital hearing loss; 4. History of ear barometric injury or trauma; 5. History of drug-induced deafness or syphilitic deafness; 6. Diabetes mellitus combined with diabetic foot, diabetic nephropathy, diabetic retinopathy, cerebral hemorrhage, and cerebrovascular embolism history; 7. Combined with active phase of tuberculosis, rheumatic disease, severe coronary atherosclerosis, severe psychosis, and pancreatitis; 8. Patients with chronic renal insufficiency, severe osteoporosis, alcoholism, head and neck malignant tumor and history of radiotherapy and chemotherapy; 9. Combined immunodeficiency virus, hepatitis B virus, hepatitis C virus, herpes zoster virus infection; 10. Chemotherapy drugs or immunosuppressants were used within the first two weeks; 11. The drug allergies involved in the trial.

Design outcomes

Primary

MeasureTime frame
Pure tone average, PTA;

Countries

China

Contacts

Public ContactWeiqiang Yang

Peking Unversity Shenzhen hospital

497450210@qq.com+86 13510818236

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026