Balloon Eustachian Tuboplasty-A Feasible Double-Blinded Sham Surgery Randomized Clinical Trial Protocol to Study Efficacy

dc.contributor.authorLaakso Juha T
dc.contributor.authorOehlandt Heidi
dc.contributor.authorKivekäs Ilkka
dc.contributor.authorHarju Teemu
dc.contributor.authorJero Jussi
dc.contributor.authorSinkkonen Saku T
dc.contributor.organizationfi=korva-, nenä-, ja kurkkutautioppi|en=Otorhinolaryngology - Head and Neck Surgery|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.93326749889
dc.contributor.organization-code2607312
dc.converis.publication-id181412502
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/181412502
dc.date.accessioned2025-08-27T21:54:15Z
dc.date.available2025-08-27T21:54:15Z
dc.description.abstract<p><strong>Introduction: </strong>Balloon Eustachian tuboplasty (BET) is used to treat obstructive Eustachian tube dysfunction (OETD) and recurrent otitis media with effusion (OME). However, there are no indisputable evidence of its efficacy. Here, we present a multicenter, double-blinded, randomized, placebo-controlled trial (MDRCT) design to evaluate the efficacy of BET, and the results of a pilot trial with 3- and 12-months' follow-up.</p><p><strong>Material and methods: </strong>This was a prospective MDRCT. For a pilot study, OETD (n = 10) and OME (n = 5) patients were recruited and followed. Detailed inclusion and exclusion criteria were used. Participants were randomized at beginning of the operation to active or sham surgery. All procedures were performed under local anesthesia. Controls were performed in double-blinded manner (both patient and physician), at 3 and 12 months after the procedure.</p><p><strong>Results: </strong>Altogether, 20 ears were treated and followed for 12 months, including 14 active BETs and 6 sham surgeries. Both the active and sham surgery were performed under local anesthesia without problems or deviations from the protocol. There were no differences in the preoperative symptoms (ETDQ-7) or objective measures (tympanometry, Valsalva and Toynbee maneuvers, tubomanometry, Eustachian tube score) between active and sham surgery arms. During follow-up, we noticed largely similar reduction in subjective symptoms and improvement in Eustachian tube score both in active and sham surgery arms.</p><p><strong>Conclusions: </strong>The pilot study demonstrates that our MDRCT protocol is feasible, and that blinded RCTs are dearly needed to objectively measure the efficacy of BET.</p><p><strong>Level of evidence: </strong>2 Laryngoscope, 2023.</p>
dc.identifier.jour-issn0023-852X
dc.identifier.olddbid201371
dc.identifier.oldhandle10024/184398
dc.identifier.urihttps://www.utupub.fi/handle/11111/48202
dc.identifier.urlhttps://doi.org/10.1002/lary.31092
dc.identifier.urnURN:NBN:fi-fe2025082785346
dc.language.isoen
dc.okm.affiliatedauthorOehlandt, Heidi
dc.okm.affiliatedauthorJero, Jussi
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3125 Otorhinolaryngology, ophthalmologyen_GB
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3125 Korva-, nenä- ja kurkkutaudit, silmätauditfi_FI
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWILEY
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1002/lary.31092
dc.relation.ispartofjournalLaryngoscope
dc.source.identifierhttps://www.utupub.fi/handle/10024/184398
dc.titleBalloon Eustachian Tuboplasty-A Feasible Double-Blinded Sham Surgery Randomized Clinical Trial Protocol to Study Efficacy
dc.year.issued2023

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