NCT01857765撤回不适用
How Rehabilitation Affects the Time to Pain-free Living After Endoscopic Transaxillary Subpectoral Breast Augmentation
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- Time to return to baseline as measured on Visual Analogue Scale for pain
研究概览
简要总结
The purpose of this study is to determine whether implementing a rehabilitation program can improve the post-operative time to pain free living after breast augmentation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •women who undergo endoscopic transaxillary subpectoral breast augmentation
- •women above the age of 18 years
- •women with a BMI 18-27
排除标准
- •women who underwent previous breast reconstruction (cosmetic or therapeutic)
- •women who underwent previous chest surgery
- •women with previous chest trauma
- •women who underwent previous shoulder/arm surgery
- •women with previous shoulder/arm injury
- •women who smoke
- •women who are Immunocompromised
结局指标
主要结局
Time to return to baseline as measured on Visual Analogue Scale for pain
时间窗: Baseline, six months, and one year after surgery
次要结局
- Time to return to bilateral shoulder baseline range of motion(Baseline, six months, and one year after surgery)
- Change in psychosocial outcomes as measured by the BREAST-Q questionnaire(Baseline, six months, and one year after surgery)
研究者
研究点 (1)
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