Protocol for a multicentre randomised controlled trial of STeroid Administration Routes For Idiopathic Sudden sensorineural Hearing loss: The STARFISH trial.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 17 08 2023
accepted: 08 12 2023
medline: 29 2 2024
pubmed: 29 2 2024
entrez: 29 2 2024
Statut: epublish

Résumé

Idiopathic sudden sensorineural hearing loss (ISSNHL) is the rapid onset of reduced hearing due to loss of function of the inner ear or hearing nerve of unknown aetiology. Evidence supports improved hearing recovery with early steroid treatment, via oral, intravenous, intratympanic or a combination of routes. The STARFISH trial aims to identify the most clinically and cost-effective route of administration of steroids as first-line treatment for ISSNHL. STARFISH is a pragmatic, multicentre, assessor-blinded, three-arm intervention, superiority randomised controlled trial (1:1:1) with an internal pilot (ISRCTN10535105, IRAS 1004878). 525 participants with ISSNHL will be recruited from approximately 75 UK Ear, Nose and Throat units. STARFISH will recruit adults with sensorineural hearing loss averaging 30dBHL or greater across three contiguous frequencies (confirmed via pure tone audiogram), with onset over a ≤3-day period, within four weeks of randomisation. Participants will be randomised to 1) oral prednisolone 1mg/Kg/day up to 60mg/day for 7 days; 2) intratympanic dexamethasone: three intratympanic injections 3.3mg/ml or 3.8mg/ml spaced 7±2 days apart; or 3) combined oral and intratympanic steroids. The primary outcome will be absolute improvement in pure tone audiogram average at 12-weeks following randomisation (0.5, 1.0, 2.0 and 4.0kHz). Secondary outcomes at 6 and 12 weeks will include: Speech, Spatial and Qualities of hearing scale, high frequency pure tone average thresholds (4.0, 6.0 and 8.0kHz), Arthur Boothroyd speech test, Vestibular Rehabilitation Benefit Questionnaire, Tinnitus Functional Index, adverse events and optional weekly online speech and pure tone hearing tests. A health economic assessment will be performed, and presented in terms of incremental cost effectiveness ratios, and cost per quality-adjusted life-year. Primary analyses will be by intention-to-treat. Oral prednisolone will be the reference. For the primary outcome, the difference between group means and 97.5% confidence intervals at each time-point will be estimated via a repeated measures mixed-effects linear regression model.

Identifiants

pubmed: 38422002
doi: 10.1371/journal.pone.0290480
pii: PONE-D-23-24534
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0290480

Informations de copyright

Copyright: © 2024 Smith et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Matthew E Smith (ME)

University of Cambridge, Cambridge, United Kingdom.
Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

Rachel Knappett (R)

Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

Deborah Vickers (D)

University of Cambridge, Cambridge, United Kingdom.

David White (D)

Patient Advocate, United Kingdom.

Chris J Schramm (CJ)

Independent General Practitioner, NHS General Practice, United Kingdom.

Samir Mehta (S)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Yongzhong Sun (Y)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Ben Watkins (B)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Marie Chadburn (M)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Hugh Jarrett (H)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Karen James (K)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Elizabeth Brettell (E)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Tracy E Roberts (TE)

Birmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.

Manohar L Bance (ML)

University of Cambridge, Cambridge, United Kingdom.
Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

James R Tysome (JR)

University of Cambridge, Cambridge, United Kingdom.
Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

Classifications MeSH