NCT07814677

Brief Summary

Safety and efficacy of intracochlear injection of glucocorticoid through the round window membrane in patients with profound or complete sudden sensorineural hearing loss

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
56

participants targeted

Target at P25-P50 for phase_2

Timeline
26mo left

Started Sep 2026

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress2%
Sep 2026Dec 2028

First Submitted

Initial submission to the registry

September 6, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 11, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

September 15, 2026

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 15, 2028

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2028

Last Updated

September 11, 2026

Status Verified

September 1, 2026

Enrollment Period

2.2 years

First QC Date

September 6, 2026

Last Update Submit

September 6, 2026

Conditions

Keywords

intracochlear injectionglucocorticoidround window membrane

Outcome Measures

Primary Outcomes (2)

  • Change from Baseline in pure tone audiometry (PTA)

    hearing capacity of thresholds ( PTA)

    Baseline , Week2 , Week4, Week12, Week24.

  • Change from Baseline in Speech Discrimination Scores

    hearing capacity of thresholds ( speech discrimination )

    Baseline , Week4, Week12, Week24.

Secondary Outcomes (5)

  • Change from Baseline in auditory brainstem re-sponse (ABR)

    Baseline, Week12

  • Change from Baseline in auditory steady-state response (ASSR)

    Baseline, Week12

  • change from baseline in tinnitus handicap inventory

    Baseline, Week2, Week4, Week12, Week24

  • change from baseline in dizziness handicap inventory

    Baseline, Week2, Week4, Week12, Week24

  • change from baseline in quality of life score

    Baseline, Week2, Week4, Week12, Week24

Study Arms (2)

Group 1:intracochlear dexamethasone injection

EXPERIMENTAL

intracochlear injection of triamcinolone acetonide through the round window membrane

Drug: intracochlear injection of triamcinolone acetonide through the round window membrane

Group 2: intratympanic dexamethasone injection

ACTIVE COMPARATOR

intratympanic dexamethasone injection through the tympanic membrane

Drug: intratympanic dexamethasone injection through the tympanic membrane

Interventions

intracochlear injection of triamcinolone acetonide through the round window membrane

Group 1:intracochlear dexamethasone injection

intratympanic dexamethasone injection through the tympanic membrane

Group 2: intratympanic dexamethasone injection

Eligibility Criteria

Age12 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Age between 12 and 75 years Unilateral idiopathic sudden sensorineural hearing loss diagnosed by Pure tone test, CT and MRI Symptoms of sudden deafness occur within ≥ 7 days and, after conventional treatment, the average thresholds at 500 Hz, 1000 Hz, 2000 Hz and 4000 Hz are ≥ 80 dBHL

You may not qualify if:

  • Bilateral sudden sensorineural hearing loss Hearing loss with known causes (e.g., Meniere's disease, retrocochlear pathology, history of otologic surgery, perilymphatic fistula, barotrauma) History in the past 6 months of ototoxic treatment such as chemotherapy, use of loop diuretics, high dose aspirin, etc.
  • History of sudden sensorineural hearing loss within the past 2 years History of ischemic diseases (cerebral infarction, myocardial infarction, peripheral arterial obstructive disease) Neuropsychiatric disorders (epilepsy, Parkinson's disease, Alzheimer's disease, multiple sclerosis) Severe hepatic or renal insufficiency The CT diagnosis is "abnormality of the round window niche".

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Eye and ENT Hospital, Fudan University

Shanghai, Shanghai Municipality, 200031, China

Location

Related Publications (12)

  • Lv J, Wang H, Cheng X, Chen Y, Wang D, Zhang L, Cao Q, Tang H, Hu S, Gao K, Xun M, Wang J, Wang Z, Zhu B, Cui C, Gao Z, Guo L, Yu S, Jiang L, Yin Y, Zhang J, Chen B, Wang W, Chai R, Chen ZY, Li H, Shu Y. AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial. Lancet. 2024 May 25;403(10441):2317-2325. doi: 10.1016/S0140-6736(23)02874-X. Epub 2024 Jan 24.

    PMID: 38280389BACKGROUND
  • Choi JW, Lee CK, Kim SB, Lee DY, Ko SC, Park KH, Choi SJ. Potential benefits of salvage intratympanic dexamethasone injection in profound idiopathic sudden sensorineural hearing loss. Eur Arch Otorhinolaryngol. 2020 Aug;277(8):2219-2227. doi: 10.1007/s00405-020-05967-z. Epub 2020 Apr 15.

    PMID: 32296977BACKGROUND
  • Plontke SK, Biegner T, Kammerer B, Delabar U, Salt AN. Dexamethasone concentration gradients along scala tympani after application to the round window membrane. Otol Neurotol. 2008 Apr;29(3):401-6. doi: 10.1097/MAO.0b013e318161aaae.

    PMID: 18277312BACKGROUND
  • Matsui H, Lopez IA, Ishiyama G, Ishiyama A. Immunohistochemical localization of glucocorticoid receptors in the human cochlea. Brain Res. 2023 May 1;1806:148301. doi: 10.1016/j.brainres.2023.148301. Epub 2023 Mar 1.

    PMID: 36868509BACKGROUND
  • Bird PA, Begg EJ, Zhang M, Keast AT, Murray DP, Balkany TJ. Intratympanic versus intravenous delivery of methylprednisolone to cochlear perilymph. Otol Neurotol. 2007 Dec;28(8):1124-30. doi: 10.1097/MAO.0b013e31815aee21.

    PMID: 18043438BACKGROUND
  • Rauch SD, Halpin CF, Antonelli PJ, Babu S, Carey JP, Gantz BJ, Goebel JA, Hammerschlag PE, Harris JP, Isaacson B, Lee D, Linstrom CJ, Parnes LS, Shi H, Slattery WH, Telian SA, Vrabec JT, Reda DJ. Oral vs intratympanic corticosteroid therapy for idiopathic sudden sensorineural hearing loss: a randomized trial. JAMA. 2011 May 25;305(20):2071-9. doi: 10.1001/jama.2011.679.

    PMID: 21610239BACKGROUND
  • Li W, Hartsock JJ, Dai C, Salt AN. Permeation Enhancers for Intratympanically-applied Drugs Studied Using Fluorescent Dexamethasone as a Marker. Otol Neurotol. 2018 Jun;39(5):639-647. doi: 10.1097/MAO.0000000000001786.

    PMID: 29649043BACKGROUND
  • Silverstein H, Choo D, Rosenberg SI, Kuhn J, Seidman M, Stein I. Intratympanic steroid treatment of inner ear disease and tinnitus (preliminary report). Ear Nose Throat J. 1996 Aug;75(8):468-71, 474, 476 passim.

    PMID: 8828271BACKGROUND
  • Wilson WR, Byl FM, Laird N. The efficacy of steroids in the treatment of idiopathic sudden hearing loss. A double-blind clinical study. Arch Otolaryngol. 1980 Dec;106(12):772-6. doi: 10.1001/archotol.1980.00790360050013.

    PMID: 7002129BACKGROUND
  • SCHUKNECHT HF. Ablation therapy in the management of Meniere's disease. Acta Otolaryngol Suppl. 1957;132:1-42. No abstract available.

    PMID: 13457879BACKGROUND
  • Fishman JM, Cullen L. Investigating sudden hearing loss in adults. BMJ. 2018 Nov 12;363:k4347. doi: 10.1136/bmj.k4347. No abstract available.

    PMID: 30420423BACKGROUND
  • Chandrasekhar SS, Tsai Do BS, Schwartz SR, Bontempo LJ, Faucett EA, Finestone SA, Hollingsworth DB, Kelley DM, Kmucha ST, Moonis G, Poling GL, Roberts JK, Stachler RJ, Zeitler DM, Corrigan MD, Nnacheta LC, Satterfield L, Monjur TM. Clinical Practice Guideline: Sudden Hearing Loss (Update) Executive Summary. Otolaryngol Head Neck Surg. 2019 Aug;161(2):195-210. doi: 10.1177/0194599819859883.

    PMID: 31369349BACKGROUND

MeSH Terms

Conditions

Hearing Loss, Sudden

Condition Hierarchy (Ancestors)

Hearing LossHearing DisordersEar DiseasesOtorhinolaryngologic DiseasesSensation DisordersNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Yilai Shu, MD, Ph.D

    Eye & ENT Hospital, Fudan University, Shanghai, China

    PRINCIPAL INVESTIGATOR
  • Huawei Li, MD, Ph.D

    Eye & ENT Hospital, Fudan University, Shanghai, China

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Wei Li, MD, Ph.D

CONTACT

Wuqing Wang, MD, Ph.D

CONTACT

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Parallel Assignment
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 6, 2026

First Posted

September 11, 2026

Study Start

September 15, 2026

Primary Completion (Estimated)

November 15, 2028

Study Completion (Estimated)

December 15, 2028

Last Updated

September 11, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

The ethics committee may require approval for data sharing to ensure alignment with principles like beneficence and justice.

Locations