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The Effects of Autologous Fat Transfer on Preventing Expanded Skin From Expansion Failure

2016年6月17日 更新者:Qing-FengLi Li,MD、Shanghai Jiao Tong University School of Medicine
The purpose of this study is to evaluate whether autologous fat grafting is safe and/or effective to prevent expanded skin from expansion failure.

研究概览

地位

完全的

条件

详细说明

The repair of skin defects is a common problem for reconstructive surgeons.Soft tissue expansion is a widely used technique for the repair of skin defects. Early expansion-related complications such as skin thinning, telangiectasia, and striae may result in expansion failure and ultimately jeopardize final outcome. In the past years, discontinuation of the expansion procedure was the only therapeutic option, when early alarm signs such as semitransparent appearance and telangiectasia of the expanded skin were encountered. We aimed to overcome these complications by therapeutic fat grafting to prevent skin necrosis and enable continuation of the expansion procedure.

Patients undergoing soft tissue expansion treatment for resurfacing skin lesions including scars and nevi that required therapeutic intervention due to early complication signs were included in this study. Patients were randomly divided into treatment group using autologous fat grafting and control group with discontinued expansion and expectant management. The treatment group received autologous fat transfer to the expanded skin.

研究类型

介入性

注册 (实际的)

80

阶段

  • 阶段2
  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Shanghai、中国
        • Shanghai Ninth People's Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 60年 (成人)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Expanding skin donor site at the face, neck, anterior chest wall, abdominal wall or back;
  • Implanted silicone expander of 50 to 800 ml in size;
  • History of deterioration in the expanded skin texture that did not improve after the inflation procedure was suspended for more than 2 weeks;
  • Persistent high level of expander internal pressure;
  • Need for further skin expansion;

Exclusion Criteria:

  • Evidence of infection, ischemia, ulcer or other pathological changes within the targeting area which defined as not suitable for expansion; or history of delayed healing, radiational therapy;
  • Rupture of expanded skin, expander exposure;
  • Significant renal, cardiovascular, hepatic and psychiatric diseases;
  • Significant medical diseases or infection (including but not limited to the carrier of hepatitis B virus or HIV);
  • BMI less than 17 or insufficient subcutaneous fat;
  • History of any hematological disease, including leukopenia , thrombocytopenia, or thrombocytosis;
  • History of allogenic bone marrow transplantation;
  • Pregnant or lactating woman;
  • Long history of smoking;
  • Evidence of malignant diseases or unwillingness to participate

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:Experimental: Fat grafting
Autologous fat graft transplantation subdermally to expanded skin.
In the experimental group, liposuction will be performed and autologous fat graft will be harvest after washing with saline. Patients will receive autologous fat graft transplantation subdermally to expanded skin.
无干预:Control
Expansion was discontinued until the early signs of complication disappeared.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
To Measure the Change in Expansion Volume
大体时间:Change from baseline volume at 12 weeks
Record the volume(ml) of each expander
Change from baseline volume at 12 weeks
To Measure the Change in Skin Thickness
大体时间:Change from baseline skin thickness at 12 weeks
Record the thickness of the expanded skin(cm) by ultrasound scanning
Change from baseline skin thickness at 12 weeks

次要结果测量

结果测量
措施说明
大体时间
To Measure the Texture of Expanded Flap with VISIA scanner
大体时间:baseline and 12 weeks post treatment
Evaluate skin texture with VISIA scanner and compare the characteristics
baseline and 12 weeks post treatment
Occurence of Major Adverse Events
大体时间:Up to approximately 12 weeks after study start
Including expanded flap ischaemia, necrosis, fluidify, infection, and all other adverse events
Up to approximately 12 weeks after study start

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2011年1月1日

初级完成 (实际的)

2016年3月1日

研究完成 (实际的)

2016年5月1日

研究注册日期

首次提交

2016年6月5日

首先提交符合 QC 标准的

2016年6月17日

首次发布 (估计)

2016年6月22日

研究记录更新

最后更新发布 (估计)

2016年6月22日

上次提交的符合 QC 标准的更新

2016年6月17日

最后验证

2016年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • Shanghai9PH

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

Fat grafting的临床试验

3
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