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Combining sound with tongue stimulation for the treatment of tinnitus: a multi-site single-arm controlled pivotal trial.
Boedts, Michael; Buechner, Andreas; Khoo, S Guan; Gjaltema, Welmoed; Moreels, Frederique; Lesinski-Schiedat, Anke; Becker, Philipp; MacMahon, Helen; Vixseboxse, Lieke; Taghavi, Razieh; Lim, Hubert H; Lenarz, Thomas.
Afiliação
  • Boedts M; BRAI3N Clinic, Gent, Belgium.
  • Buechner A; Maria Middelares General Hospital, Gent, Belgium.
  • Khoo SG; Department of Otolaryngology, Hannover Medical School, Hannover, Germany.
  • Gjaltema W; German Hearing Center (DHZ), Hannover Medical School, Hannover, Germany.
  • Moreels F; St. James's Hospital, Dublin, Ireland.
  • Lesinski-Schiedat A; St. Vincent's Hospital, Dublin, Ireland.
  • Becker P; Avania, Bilthoven, The Netherlands.
  • MacMahon H; BRAI3N Clinic, Gent, Belgium.
  • Vixseboxse L; Department of Otolaryngology, Hannover Medical School, Hannover, Germany.
  • Taghavi R; German Hearing Center (DHZ), Hannover Medical School, Hannover, Germany.
  • Lim HH; German Hearing Center (DHZ), Hannover Medical School, Hannover, Germany.
  • Lenarz T; Otologie Clinic, Dublin, Ireland.
Nat Commun ; 15(1): 6806, 2024 Aug 19.
Article em En | MEDLINE | ID: mdl-39160146
ABSTRACT
Bimodal neuromodulation is emerging as a nonsurgical treatment for tinnitus. Bimodal treatment combining sound therapy with electrical tongue stimulation using the Lenire device is evaluated in a controlled pivotal trial (TENT-A3, NCT05227365) consisting of 6-weeks of sound-only stimulation (Stage 1) followed by 6-weeks of bimodal treatment (Stage 2) with 112 participants serving as their own control. The primary endpoint compares the responder rate observed in Stage 2 versus Stage 1, where a responder exceeds 7 points in the Tinnitus Handicap Inventory. In participants with moderate or more severe tinnitus, there is a clinically superior performance of bimodal treatment (58.6%; 95% CI 43.5%, 73.6%; p = 0.022) compared to sound therapy alone (43.2%; 95% CI 29.7%, 57.8%), which is not observed in the full cohort across all severity groups. Consistent results are observed for the secondary endpoint based on the Tinnitus Functional Index (bimodal treatment 45.5%; 95% CI 31.7%, 59.9%; sound-only stimulation 29.6%; 95% CI 18.2%, 44.2%; p = 0.010), where a responder exceeds 13 points. There are no device related serious adverse events. These positive outcomes led to FDA De Novo approval of the Lenire device for tinnitus treatment.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Zumbido / Língua Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Zumbido / Língua Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica