跳至主要内容
临床试验/NCT07704372
NCT07704372尚未招募2 期

Superoxide Dismutase Skin Spray for Reducing Acute Radiation Dermatitis in Patients With Head and Neck Cancer Undergoing Radiotherapy: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial

West China Hospital1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2026年7月15日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
尚未招募
入组人数
140
试验地点
1
主要终点
Incidence of grade ≥ 2 ARD

研究概览

简要总结

To evaluate the efficacy and safety of superoxide dismutase skin spray for the reducing the acute radiation dermatitis in patients with head and neck malignancies undergoing radiotherapy.

详细描述

Radiotherapy (RT) is a cornerstone treatment for patients with head and neck cancer and may be administered as definitive, adjuvant, or concurrent therapy with chemotherapy depending on disease stage and clinical indication. Despite its therapeutic benefits, RT is frequently associated with a range of acute toxicities, among which radiation dermatitis is one of the most common and clinically relevant adverse effects. Radiation-induced skin injury may present during or shortly after the course of radiotherapy and can significantly impact patient comfort, treatment adherence, and overall quality of life. Severe cases may lead to treatment interruption or dose modification, potentially compromising oncologic outcomes. The incidence of acute radiation dermatitis in patients with head and neck cancer has been reported to be high, with a substantial proportion of patients developing at least moderate-grade skin reactions during the course of radiotherapy. However, current preventive and therapeutic strategies remain limited, and no universally accepted standard of care has been established. Existing supportive measures are primarily empirical and have shown variable efficacy in reducing the severity or progression of skin toxicity. Superoxide dismutase (SOD) is an endogenous antioxidant enzyme with the ability to catalyze the dismutation of superoxide radicals into oxygen and hydrogen peroxide, thereby reducing oxidative stress-induced cellular damage. Given that oxidative stress is a key mechanism underlying radiation-induced skin injury, topical application of SOD-based formulations may provide a biologically plausible approach for mitigating radiation dermatitis. Based on this rationale, the present clinical trial is designed to investigate the efficacy and safety of a topical SOD skin spray in preventing and reducing acute radiation dermatitis in patients with head and neck cancer undergoing radiotherapy.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically confirmed malignant tumors of the head and neck without distant metastasis.
  • Scheduled to undergo either postoperative adjuvant radiotherapy or definitive radiotherapy, with or without concurrent chemotherapy.
  • Age 18-80 years at the time of consent.
  • Eastern Cooperative Oncology Group (ECOG) performance status 0-
  • Signed informed consent form.
  • Adequate cognitive and reading abilities to complete the questionnaire.

排除标准

  • Pre-existing skin disease or open wounds in the irradiation field.
  • Have a history of head and neck radiotherapy.
  • Autoimmune or connective tissue disorders affecting skin.
  • Known allergy to any component of study formulations.
  • Any condition that, in the investigator's judgment, would interfere with study participation or outcome assessment.

结局指标

主要结局

Incidence of grade ≥ 2 ARD

时间窗: From the start of radiotherapy to 4 weeks after completion of radiotherapy

Patients are assessed weekly for radiation dermatitis by an experienced radiation oncology nurse according to the Radiation Therapy Oncology Group (RTOG) scale. The RTOG scale categorizes acute skin toxicity into grades 0-4, with the higher the grade the more severe the patient's acute radiation dermatitis. Grade 0 means no change over baseline. Grade 1 means follicular, faint, or dull erythema; epilation, dry desquamation, or decrease in sweating. Grade 2 means tender, bright erythema; patchy, moist desquamation or moderate edema. Grade 3 means confluent, moist desquamation other than skin folds; pitting edema. Grade 4 means ulceration, hemorrhage, necrosis.

次要结局

  • Time to onset of grade ≥ 2 ARD between the two arms.(From the start of radiotherapy to 4 weeks after completion of radiotherapy.)
  • Duration of grade ≥ 2 ARD between the two arms.(From the start of radiotherapy to 4 weeks after completion of radiotherapy.)
  • Maximum dermatitis grade(From the start of radiotherapy to 4 weeks after completion of radiotherapy.)
  • Grade ≥3 radiation dermatitis incidence(From the start of radiotherapy to 4 weeks after completion of radiotherapy.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xingchen Peng

PhD, Professor

West China Hospital

研究点 (1)

Loading locations...

相似试验