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Risk Factor Analysis and Construction and Application of Intelligent Prediction Model for Sudden Sensorineural Hearing Loss

Risk Factor Analysis and Construction and Application of Intelligent Prediction Model for Sudden Sensorineural Hearing Loss

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129767
Enrollment
Unknown
Registered
2026-08-10
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-08-24

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

Conditions

Idiopathic sudden sensorineural hearing loss,ISSNHL

Interventions

Control group:None

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for idiopathic sudden hearing loss according to the "Guidelines for the Diagnosis and Treatment of Sudden Deafness": sudden, unexplained sensorineural hearing loss within 72 hours, with a hearing drop of >=20 dBHL at two consecutive frequencies; pure-tone audiometry types include flat loss or total deafness (hearing loss across all frequencies); 2. Hospitalized in the ENT department of our hospital for standardized treatment; 3. After treatment, follow-up pure-tone audiometry is done, with complete hearing follow-up results available to assess hearing recovery prognosis.

Exclusion criteria

Exclusion criteria: 1. There are conductive problems in the middle ear (like otitis media, eardrum perforation, otosclerosis, etc.), with an air-bone gap >10dB indicated by tympanometry; 2. There are clear secondary causes of hearing loss: acoustic neuroma, head trauma, exposure to ototoxic drugs, Ménière's disease, or congenital permanent hearing impairment; 3. Accompanied by end-stage liver or kidney failure, malignant tumors, congenital bleeding disorders, or autoimmune inner ear disease; 4. Interrupted standard treatment during hospitalization or discharged early before completing the standard care process.

Design outcomes

Primary

MeasureTime frame
After one course of treatment (7 days), the improvement in average pure-tone audiometry (PTA) threshold at outpatient follow-up;

Secondary

MeasureTime frame
Blood clotting test indicators;Blood lipid indicators;

Countries

China

Contacts

Public ContactLei Yu

The First Affiliated Hospital of Dalian Medical University

leiyu@firsthosp-dmu.com+86 411 8363 5963

Outcome results

None listed

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