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临床试验/NCT02443493
NCT02443493已完成不适用

Low-level Laser Therapy as a Tool for the Prevention of Radiodermatitis in Breast Cancer Patients

Hasselt University2 个研究点 分布在 1 个国家目标入组 139 人开始时间: 2015年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
139
试验地点
2
主要终点
Radiation Dermatitis Grade

研究概览

简要总结

Up to 90% of the radiotherapy patients will develop a certain degree of skin reaction at the treated area, also known as radiodermatitis (RD).

Currently, there is a wide variety of strategies to manage RD, including creams, gels, ointments, wound dressings. However, up to now, there is still no comprehensive, evidence-based consensus for the treatment of RD. Low-level laser therapy (LLLT) is a promising, non-invasive technique for treating RD. In a recent pilot study conducted in our research group, LLLT prevented the aggravation of RD and provided symptomatic relief in patients undergoing radiotherapy for breast cancer after breast-sparing surgery. This pilot study was the first prospective study investigating the potential of LLLT for RD. In the current study, we want to investigate the efficacy of LLLT as a tool for the prevention of radiodermatitis in breast cancer patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

入排标准

性别
Female
接受健康志愿者

入选标准

  • Diagnosis of non-invasive (stage 0) or invasive (stage 1, 2 and 3A) breast adenocarcinoma
  • Treatment with primary breast-sparing surgery (lumpectomy) and/or neoadjuvant (preoperative) or adjuvant (postoperative) chemotherapy or hormonal therapy
  • Scheduled for postoperative radiotherapy with standard technique (isocentric) and fractionation regime (i.e. 25 daily fractions of 2 Gray to the whole breast followed by a boost of 8 fractions of 2 Gray to the tumor bed, 5/week)
  • Signed informed consent

排除标准

  • Previous irradiation to the same breast
  • Metastatic disease
  • Concurrent chemotherapy
  • Required use of bolus material to deliver radiotherapy (i.e. material placed on the to- be-irradiated zone to modulate the delivered dose in order the ensure an optimal distribution of the radiation dose; mostly used for treatment of superficial tumors)

研究组 & 干预措施

Treatment group

Experimental

Treatment group (receives low-level laser therapy (2x/week) in combination with standard skin care starting from day 1 of radiotherapy)

干预措施: Low-level laser (Device)

Treatment group

Experimental

Treatment group (receives low-level laser therapy (2x/week) in combination with standard skin care starting from day 1 of radiotherapy)

干预措施: radiotherapy (Radiation)

Control group

Sham Comparator

Control group (receives sham laser (2x/week) in combination with standard skin care starting from day 1 of radiotherapy)

干预措施: sham laser (Device)

Control group

Sham Comparator

Control group (receives sham laser (2x/week) in combination with standard skin care starting from day 1 of radiotherapy)

干预措施: radiotherapy (Radiation)

结局指标

主要结局

Radiation Dermatitis Grade

时间窗: day 54

objective scoring of the severity of radiation dermatitis using the grading system of the Radiation Therapy Oncology Group/ European Organization for Research and Treatment of Cancer (RTOG/ EORTC)

Radiation Dermatitis Assessment

时间窗: day 54

radiation dermatitis assessment scale (Radiation-Induced Skin Reaction Assessment Scale, RISRAS)

Objective measurement of the skin hydration

时间窗: day 40

Corneo meter CM825 will be used to objectively assess the skin barrier function by measuring the skin hydration

Objective measurement of degree of erythema of the skin

时间窗: day 54

Mexa meter MX18 will be used to objectively measure the degree of erythema of the skin

Analyze the skin cytokine content of the irradiated and non-irradiated breast

时间窗: day 54

Collect skin tape samples of the irradiated and non-irradiated breast in order to analyze these samples on cytokines by ELISA

Objective measurement of trans epidermal water loss of the skin

时间窗: day 54

Tewa meter TM 300 will be used to objectively assess the skin barrier function by measuring the trans epidermal water loss of the skin

次要结局

  • Satisfaction with therapy(day 54)
  • moist desquamation(day 54)
  • Pain(day 54)
  • Quality of life(day 54)

研究者

发起方
Hasselt University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. dr. Jeroen Mebis

prof. dr.

Hasselt University

研究点 (2)

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