dc.contributor.author
Linares-Gil, M.J.
dc.contributor.author
Valls Marsal, Joan
dc.contributor.author
Hereu-Boher, P.
dc.contributor.author
Nebot, F.J.
dc.contributor.author
De-Ramón, B.
dc.contributor.author
Diaz-Munió, E.
dc.contributor.author
Sanzol, R.
dc.contributor.author
De-Oca, J.
dc.contributor.author
Pérez-Lozano, P.
dc.contributor.author
Suñé-Negre, J.M.
dc.contributor.author
García-Montoya, E.
dc.date.accessioned
2024-12-05T22:12:36Z
dc.date.available
2024-12-05T22:12:36Z
dc.date.issued
2020-06-16T10:03:19Z
dc.date.issued
2020-06-16T10:03:19Z
dc.identifier
https://doi.org/10.1038/s41424-018-0075-7
dc.identifier
http://hdl.handle.net/10459.1/69022
dc.identifier.uri
http://hdl.handle.net/10459.1/69022
dc.description.abstract
Objective: The aim of this study is to evaluate the efficacy and safety of a topical formulation containing lidocaine plus diclofenac (CLIFE1) compared to lidocaine (CLIFE2), to decrease pain in benign anorectal surgery (BARS) to date not evaluated. More than 50% of patients undergoing BARS, especially hemorrhoidectomy, suffer from moderate and severe postoperative pain. This remains an unresolved problem that could be addressed with the new CLIFE1 topical treatment.
Methods: A multicenter, randomized double-blind, active-controlled parallel-group superiority trial, was conducted in two Spanish hospitals. Patients undergoing BARS (hemorrhoids, anal fistula and anal fissure) were randomized at the end of surgery at a 1:1 ratio to receive first dose either CLIFE1 (n = 60) or CLIFE2 (n = 60) anorectal topical treatment, and after every 12 h for the first three postoperative days and once a day from the fourth to sixth. The primary outcome was average of pain decrease after topical treatment, measured with visual analogue scale (VAS) by the patients themselves, the evening in the surgery day and four times daily for the first three postoperative days.
Results: The results of 120 patients included out of 150 selected undergoing BARS show a decrease in pain after CLIFE1 topical treatment (7.47 ± 13.09) greater than with CLIFE2 (4.38 ± 6.75), difference -3.21 95% CI (-5.75; -0.68), p = 0.008, decreasing significantly postoperative pain ( ≥ 9 mm, VAS) in 35% of patients undergoing benign anorectal surgery, compared to 18.33 % treated with lidocaine.
Conclusions: The CLIFE1 topical treatment shows better analgesic efficacy than CLIFE2 in BARS.
dc.description.abstract
All these public institutions have collaborated funding the study through a competitive grant process yet the work has been completely independent from the fund sources. The Department of Health, Social and Equality Services of Spain and the Carlos III Health. Institute funded the project through a competitive public tender. ACCIO (Government of CatalunyaACCIO, Generalitat de Catalunya). European Regional Development Fund, ERDF (Fondo Europeo de Desarrollo Regional, FEDER). CERCA (Centres de Recerca de Catalunya).
dc.publisher
American College of Gastroenterology
dc.relation
Reproducció del document publicat a https://doi.org/10.1038/s41424-018-0075-7
dc.relation
Clinical and Translational Gastroenterology, 2018, vol. 9, núm. 11, p. 210
dc.rights
cc-by-nc-sa, (c) Linares-Gil et al., 2018
dc.rights
info:eu-repo/semantics/openAccess
dc.rights
http://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subject
Anus -- Cirurgia
dc.subject
Recte -- Cirurgia
dc.title
Topical Analgesia with Lidocaine Plus Diclofenac Decreases Pain in Benign Anorectal Surgery: Randomized, Doubleblind, and Controlled Clinical Trial
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion