Skin closUre in carPal tunnEl Release (SUPER): protocol for a blinded randomised controlled trial comparing absorbable and non-absorbable sutures in carpal tunnel release.

Autor:	Savolainen A; University of Eastern Finland School of Medicine, Kuopio, Finland aukusa@student.uef.fi., Nietosvaara Y; University of Eastern Finland School of Medicine, Kuopio, Finland.; Department of Orthopaedics, Traumatology and Hand Surgery, Kuopio University Hospital, Kuopio, Finland., Sirola J; University of Eastern Finland School of Medicine, Kuopio, Finland.; Kuopio University Hospital, Kuopio, Finland., Hytönen M; University of Eastern Finland School of Medicine, Kuopio, Finland., Reito A; Department of Orthopaedics and Traumatology, Tampere University Hospital, Tampere, Finland., Heikkinen N; University of Eastern Finland School of Medicine, Kuopio, Finland., Räisänen MP; Department of Orthopaedics, Traumatology and Hand Surgery, Kuopio University Hospital, Kuopio, Finland.; Tampere Universities, Tampere, Finland.
Jazyk:	angličtina
Zdroj:	BMJ open [BMJ Open] 2024 Apr 16; Vol. 14 (4), pp. e082289. Date of Electronic Publication: 2024 Apr 16.
DOI:	10.1136/bmjopen-2023-082289
Abstrakt:	Introduction: Carpal tunnel syndrome is a common disorder affecting a substantial portion of the general population. Surgical intervention is often deemed necessary, with the median nerve release being one of the most frequent operations. Optimising all the aspects of this procedure can enhance patient satisfaction with the treatment. Methods and Analysis: We aim to determine the differences in the aesthetic outcome of the scar as well as the pain experienced during the healing process between the use of absorbable and non-absorbable sutures. The primary outcome measure will be the patients' subjective satisfaction with the aesthetic appearance of the scar 1 year after the operation. Secondary outcomes will include a similar evaluation of the aesthetics performed by a blinded outcome assessor, as well as pain experienced by the patients during the 2 weeks postoperatively. The severity and improvement of the patients' symptoms will also be measured by a Finnish version of the Boston Carpal Tunnel Questionnaire. Costs will be evaluated for both groups. Safety of the wound closure will be followed and reported. Ethics and Dissemination: This protocol was approved by the Research Ethics Committee of the Northern Savo Hospital District (2319/2021). The trial will be conducted in accordance with the principles of Good Clinical Practice and the Declaration of Helsinki. The results will be disseminated through publication in peer-reviewed journals. Trial Registration Number: NCT05503719. Competing Interests: Competing interests: AS, YN, AR, JS, MH and NH—none. MPR—hand and wrist course, Arthrex. (© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
Databáze:	MEDLINE
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