Scandinavian Olecranon Research in the Elderly (SCORE): protocol for a non- inferiority, randomised, controlled, multicentre trial comparing operative and conservative treatment of olecranon fractures in the elderly

dc.contributor.authorRantalaiho Ida
dc.contributor.authorLaaksonen Inari
dc.contributor.authorLaunonen Antti P
dc.contributor.authorLuokkala Toni
dc.contributor.authorFlinkkilä Tapio
dc.contributor.authorSalmela Mikko
dc.contributor.authorAdolfsson L
dc.contributor.authorOlsen Bo
dc.contributor.authorIsotalo Kari
dc.contributor.authorRyösä Anssi
dc.contributor.authorÄärimaa Ville
dc.contributor.authorSCORE study group
dc.contributor.organizationfi=kliininen laitos|en=Department of Clinical Medicine|
dc.contributor.organizationfi=ortopedia ja traumatologia|en=Orthopaedics and Traumatology|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.61334543354
dc.contributor.organization-code1.2.246.10.2458963.20.90281651480
dc.converis.publication-id174887069
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/174887069
dc.date.accessioned2022-10-27T12:13:17Z
dc.date.available2022-10-27T12:13:17Z
dc.description.abstract<p>Introduction <br></p><p>The incidence of olecranon fractures is growing in the elderly population. The traditional operative approach is giving way among the elderly to conservative treatment, which seems to provide a comparable functional outcome with a lower complication burden. However, there is still a lack of reliable evidence to support this shift.The objective of this trial is to investigate whether conservative treatment of displaced olecranon fractures in patients aged 75 or older yields comparable results to those of operative treatment in terms of pain and daily function.<br></p><p>Methods and analysis <br></p><p>Scandinavian Olecranon Research in the Elderly (SCORE) is a randomised, controlled, multicentre, non-inferiority trial. Eligible patients will be randomised to either conservative or operative treatment. The sample size will be 68 patients and allocation done at a 1:1 ratio (34 patients per group). The randomisation is stratified according to the participating hospital and patient's sex. Both groups will receive the same postoperative physiotherapy and pain management. The primary outcome is Disabilities of the Arm, Shoulder and Hand at 1-year follow-up. Secondary outcomes are pain and satisfaction measured on visual analogue scales, Patient Reported Elbow Evaluation, range of motion of the elbow and extension strength of the elbow compared with the unaffected arm. Radiographs will be taken at each follow-up. Primary analysis of the results will be conducted on an intention-to-treat basis.<br></p><p>Ethics and dissemination <br></p><p>The study protocol for this clinical trial has been approved by the Ethics Committee of the Hospital District of Southwest Finland and will be submitted for approval to the Regional Ethics Committees in Linkoping, Sweden and Copenhagen, Denmark. Every recruiting centre will apply local research approvals. The results of this study will be submitted for publication in peer-reviewed journals.</p>
dc.identifier.jour-issn2044-6055
dc.identifier.olddbid174015
dc.identifier.oldhandle10024/157109
dc.identifier.urihttps://www.utupub.fi/handle/11111/33368
dc.identifier.urlhttps://bmjopen.bmj.com/content/12/1/e055097
dc.identifier.urnURN:NBN:fi-fe2022081153812
dc.language.isoen
dc.okm.affiliatedauthorRantalaiho, Ida
dc.okm.affiliatedauthorLaaksonen, Inari
dc.okm.affiliatedauthorIsotalo, Kari
dc.okm.affiliatedauthorRyösä, Anssi
dc.okm.affiliatedauthorÄärimaa, Ville
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3126 Surgery, anesthesiology, intensive care, radiologyen_GB
dc.okm.discipline3126 Kirurgia, anestesiologia, tehohoito, radiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherBMJ PUBLISHING GROUP
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumbere055097
dc.relation.doi10.1136/bmjopen-2021-055097
dc.relation.ispartofjournalBMJ Open
dc.relation.issue1
dc.relation.volume12
dc.source.identifierhttps://www.utupub.fi/handle/10024/157109
dc.titleScandinavian Olecranon Research in the Elderly (SCORE): protocol for a non- inferiority, randomised, controlled, multicentre trial comparing operative and conservative treatment of olecranon fractures in the elderly
dc.year.issued2022

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