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Participants will receive information orally during the consultation from the surgeon and written details via e-Boks, including a link to the electronic questionnaire. After providing oral consent, participants have a minimum of 24 h to consider before signing or refusing to sign the informed consent form at T1. Data collection and processing were approved by the Region of Southern Denmark (Journal No. 22\/9955). Approval from the Danish Health Research Ethics Committee is not required for studies involving questionnaires or observations, as they are not classified as interventions under the Committee Act (decision on non-approval project ID: S-20200137). The C-RCT are registered on\n                      \n                      (NCT05972525), with registration date: 06.08.2023. Data will be stored in the Open Patient Explorative Patient Network (OPEN), in accordance with the European General Data Protection Regulation. Authorship eligibility will follow guidelines outlined [\n                      \n                      ].","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval and consent to participate"}},{"value":"Not required.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"CV was reimbursed for travel expenses by Stryker, paid to the institution, which are unrelated to this study. All other authors declare no competing interests.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"584"}}