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Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial
BACKGROUND: Cesarean delivery has already become a very common method of delivery around the world, especially in low-income countries. Hypertrophic scars and wound infections have affected younger mothers and frustrated obstetricians for a long time. Mesenchymal stem cells (MSCs) have strong potent...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834835/ https://www.ncbi.nlm.nih.gov/pubmed/29499740 http://dx.doi.org/10.1186/s13063-018-2478-x |
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author | Fan, Dazhi Xia, Qing Wu, Shuzhen Ye, Shaoxin Liu, Li Wang, Wen Guo, Xiaoling Liu, Zhengping |
author_facet | Fan, Dazhi Xia, Qing Wu, Shuzhen Ye, Shaoxin Liu, Li Wang, Wen Guo, Xiaoling Liu, Zhengping |
author_sort | Fan, Dazhi |
collection | PubMed |
description | BACKGROUND: Cesarean delivery has already become a very common method of delivery around the world, especially in low-income countries. Hypertrophic scars and wound infections have affected younger mothers and frustrated obstetricians for a long time. Mesenchymal stem cells (MSCs) have strong potential for self-renewal and differentiation to multilineage cells. Previous studies have demonstrated that MSCs are involved in enhancing diabetic wound healing. Therefore, this study is designed to investigate the safety and efficacy of using MSCs in the treatment of Cesarean section skin scars. METHODS: This trial is a prospective, randomized, double-blind, placebo-controlled, single-center trial with three parallel groups. Ninety eligible participants will be randomly allocated to placebo, low-dose (transdermal hydrogel MSCs; 3 × 10(6) cells) or high-dose (transdermal hydrogel MSCs; 6 × 10(6) cells) groups at a 1:1:1 allocation ratio according to a randomization list, once a day for six consecutive days. Study duration will last for 6 months, comprising a 1 week run-in period and 24 weeks of follow-up. The primary aim of this trial is to compare the difference in Vancouver Scar Scale rating among the three groups at the 6th month. Adverse events, including severe and slight signs or symptoms, will be documented in case report forms. The study will be conducted at the Department of Obstetric of Southern Medical University Affiliated Maternal & Child Health Hospital of Foshan. DISCUSSION: This trial is the first investigation of the potential for therapeutic use of MSCs for the management of women’s skin scar after Cesarean delivery. The results will give us an effective therapeutic strategy to combat Cesarean section skin scars, even with uterine scarring. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02772289. Registered on 10 May 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2478-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5834835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58348352018-03-05 Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial Fan, Dazhi Xia, Qing Wu, Shuzhen Ye, Shaoxin Liu, Li Wang, Wen Guo, Xiaoling Liu, Zhengping Trials Study Protocol BACKGROUND: Cesarean delivery has already become a very common method of delivery around the world, especially in low-income countries. Hypertrophic scars and wound infections have affected younger mothers and frustrated obstetricians for a long time. Mesenchymal stem cells (MSCs) have strong potential for self-renewal and differentiation to multilineage cells. Previous studies have demonstrated that MSCs are involved in enhancing diabetic wound healing. Therefore, this study is designed to investigate the safety and efficacy of using MSCs in the treatment of Cesarean section skin scars. METHODS: This trial is a prospective, randomized, double-blind, placebo-controlled, single-center trial with three parallel groups. Ninety eligible participants will be randomly allocated to placebo, low-dose (transdermal hydrogel MSCs; 3 × 10(6) cells) or high-dose (transdermal hydrogel MSCs; 6 × 10(6) cells) groups at a 1:1:1 allocation ratio according to a randomization list, once a day for six consecutive days. Study duration will last for 6 months, comprising a 1 week run-in period and 24 weeks of follow-up. The primary aim of this trial is to compare the difference in Vancouver Scar Scale rating among the three groups at the 6th month. Adverse events, including severe and slight signs or symptoms, will be documented in case report forms. The study will be conducted at the Department of Obstetric of Southern Medical University Affiliated Maternal & Child Health Hospital of Foshan. DISCUSSION: This trial is the first investigation of the potential for therapeutic use of MSCs for the management of women’s skin scar after Cesarean delivery. The results will give us an effective therapeutic strategy to combat Cesarean section skin scars, even with uterine scarring. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02772289. Registered on 10 May 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-018-2478-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-02 /pmc/articles/PMC5834835/ /pubmed/29499740 http://dx.doi.org/10.1186/s13063-018-2478-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Fan, Dazhi Xia, Qing Wu, Shuzhen Ye, Shaoxin Liu, Li Wang, Wen Guo, Xiaoling Liu, Zhengping Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial |
title | Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial |
title_full | Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial |
title_fullStr | Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial |
title_full_unstemmed | Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial |
title_short | Mesenchymal stem cells in the treatment of Cesarean section skin scars: study protocol for a randomized, controlled trial |
title_sort | mesenchymal stem cells in the treatment of cesarean section skin scars: study protocol for a randomized, controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834835/ https://www.ncbi.nlm.nih.gov/pubmed/29499740 http://dx.doi.org/10.1186/s13063-018-2478-x |
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