Cargando…

A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures

BACKGROUND: Skin preconditioning prior to and following procedures, has previously been demonstrated to hasten and optimize healing, and decrease the symptoms and signs associated with invasive surgery. These trials involved the use of multiple topical products. In an effort to control costs and to...

Descripción completa

Detalles Bibliográficos
Autores principales: Casas, Laurie A, Claytor, R Brannon, Zeidler, Kamakshi R, Shridharani, Sachin M, Cohen, Steven R, Khanna, Julie J, Gould, Daniel J, Yates, Essie K, Lultschik, Shantel, Bell, Michaela, Widgerow, Alan D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376671/
https://www.ncbi.nlm.nih.gov/pubmed/35979375
http://dx.doi.org/10.1093/asjof/ojac054
_version_ 1784768189113040896
author Casas, Laurie A
Claytor, R Brannon
Zeidler, Kamakshi R
Shridharani, Sachin M
Cohen, Steven R
Khanna, Julie J
Gould, Daniel J
Yates, Essie K
Lultschik, Shantel
Bell, Michaela
Widgerow, Alan D
author_facet Casas, Laurie A
Claytor, R Brannon
Zeidler, Kamakshi R
Shridharani, Sachin M
Cohen, Steven R
Khanna, Julie J
Gould, Daniel J
Yates, Essie K
Lultschik, Shantel
Bell, Michaela
Widgerow, Alan D
author_sort Casas, Laurie A
collection PubMed
description BACKGROUND: Skin preconditioning prior to and following procedures, has previously been demonstrated to hasten and optimize healing, and decrease the symptoms and signs associated with invasive surgery. These trials involved the use of multiple topical products. In an effort to control costs and to increase patient compliance, a single surgical product was developed, with actives aimed at decreasing swelling, bruising, induration, and internal fibrous banding. OBJECTIVES: This multi-center trial was designed to measure the efficacy of this single product in these mentioned parameters. METHODS: A double-blind, randomized, split body, clinical study was undertaken in 29 patients involving 38 surgical procedures. Assessments included photography, biopsies, ultrasound imaging, and blinded investigator and participant assessments. RESULTS: Differentiated results between test comparator sides became apparent at postop day 10-14 (as previously observed). Thus, blinded investigator and participant assessment scores demonstrated statistical significance exclusive to the test product side at postop day 10-14 for ecchymoses and then extending to skin discoloration, edema, induration and subcutaneous fibrous banding, at weeks 3, 4, 6, and 12. Ultrasound evaluation confirmed the earlier dissolution of fibrous banding on the test side in the subcutaneous tissue at the 3-6-week postop period. In addition, biopsies assessing the pre-conditioned period prior to surgery confirmed that the topical test product stimulated a remodeled extracellular matrix without comparative changes on the opposite side. CONCLUSIONS: A single peri-surgical product designed for the use with invasive surgery produced significant differences in ecchymosis, skin discoloration, edema, induration and ongoing resolution of fibrous banding over many weeks. This study validation provides an additional adjunct to surgical procedures. LEVEL OF EVIDENCE: 2: [Image: see text]
format Online
Article
Text
id pubmed-9376671
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-93766712022-08-16 A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures Casas, Laurie A Claytor, R Brannon Zeidler, Kamakshi R Shridharani, Sachin M Cohen, Steven R Khanna, Julie J Gould, Daniel J Yates, Essie K Lultschik, Shantel Bell, Michaela Widgerow, Alan D Aesthet Surg J Open Forum Body Contouring BACKGROUND: Skin preconditioning prior to and following procedures, has previously been demonstrated to hasten and optimize healing, and decrease the symptoms and signs associated with invasive surgery. These trials involved the use of multiple topical products. In an effort to control costs and to increase patient compliance, a single surgical product was developed, with actives aimed at decreasing swelling, bruising, induration, and internal fibrous banding. OBJECTIVES: This multi-center trial was designed to measure the efficacy of this single product in these mentioned parameters. METHODS: A double-blind, randomized, split body, clinical study was undertaken in 29 patients involving 38 surgical procedures. Assessments included photography, biopsies, ultrasound imaging, and blinded investigator and participant assessments. RESULTS: Differentiated results between test comparator sides became apparent at postop day 10-14 (as previously observed). Thus, blinded investigator and participant assessment scores demonstrated statistical significance exclusive to the test product side at postop day 10-14 for ecchymoses and then extending to skin discoloration, edema, induration and subcutaneous fibrous banding, at weeks 3, 4, 6, and 12. Ultrasound evaluation confirmed the earlier dissolution of fibrous banding on the test side in the subcutaneous tissue at the 3-6-week postop period. In addition, biopsies assessing the pre-conditioned period prior to surgery confirmed that the topical test product stimulated a remodeled extracellular matrix without comparative changes on the opposite side. CONCLUSIONS: A single peri-surgical product designed for the use with invasive surgery produced significant differences in ecchymosis, skin discoloration, edema, induration and ongoing resolution of fibrous banding over many weeks. This study validation provides an additional adjunct to surgical procedures. LEVEL OF EVIDENCE: 2: [Image: see text] Oxford University Press 2022-06-10 /pmc/articles/PMC9376671/ /pubmed/35979375 http://dx.doi.org/10.1093/asjof/ojac054 Text en © 2022 The Aesthetic Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Body Contouring
Casas, Laurie A
Claytor, R Brannon
Zeidler, Kamakshi R
Shridharani, Sachin M
Cohen, Steven R
Khanna, Julie J
Gould, Daniel J
Yates, Essie K
Lultschik, Shantel
Bell, Michaela
Widgerow, Alan D
A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures
title A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures
title_full A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures
title_fullStr A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures
title_full_unstemmed A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures
title_short A Multicenter, Randomized, Double-Blind, Split-Body Clinical Trial Evaluating the Efficacy and Outcomes of a Topical Product Pre and Post Aesthetic Surgical Body Procedures
title_sort multicenter, randomized, double-blind, split-body clinical trial evaluating the efficacy and outcomes of a topical product pre and post aesthetic surgical body procedures
topic Body Contouring
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376671/
https://www.ncbi.nlm.nih.gov/pubmed/35979375
http://dx.doi.org/10.1093/asjof/ojac054
work_keys_str_mv AT casaslauriea amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT claytorrbrannon amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT zeidlerkamakshir amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT shridharanisachinm amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT cohenstevenr amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT khannajuliej amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT goulddanielj amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT yatesessiek amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT lultschikshantel amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT bellmichaela amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT widgerowaland amulticenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT casaslauriea multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT claytorrbrannon multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT zeidlerkamakshir multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT shridharanisachinm multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT cohenstevenr multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT khannajuliej multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT goulddanielj multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT yatesessiek multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT lultschikshantel multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT bellmichaela multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures
AT widgerowaland multicenterrandomizeddoubleblindsplitbodyclinicaltrialevaluatingtheefficacyandoutcomesofatopicalproductpreandpostaestheticsurgicalbodyprocedures