Actively Recruiting
Modulating the Skin Microbiome to Prevent Radiation Dermatitis in Breast Cancer
Led by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University · Updated on 2025-07-15
326
Participants Needed
1
Research Sites
59 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Acute radiation dermatitis (ARD) is the most common treatment-related adverse reaction following radiotherapy after modified radical mastectomy and/or prosthetic breast reconstruction in breast cancer patients. Moderate-to-severe ARD may compromise cosmetic outcomes and quality of life, and even impair radiotherapy efficacy. Current pharmacological prophylactic measures clinically employed - including topical corticosteroids, superoxide dismutase, and trolamine cream - demonstrate suboptimal efficacy and lack high-level evidence-based medical support. Emerging research indicates an association between cutaneous microbial homeostasis and ARD development, suggesting that maintaining skin surface acidity and modulating microecological balance may represent more effective preventive strategies. This study evaluates the efficacy and safety of a natural weak-acid macromolecular/small molecular repair cream in preventing ARD among post-operative breast cancer patients receiving radiotherapy through skin microbiome modulation. We enrolled 326 high-risk early-stage breast cancer patients scheduled for post-operative radiotherapy and randomized them to compare the superiority of the natural weak-acid repair cream versus conventional care with moisturizer. Concurrent skin microbiome sampling was performed to assess microecological changes and their impact on ARD development. The findings will provide high-level clinical evidence and theoretical basis for the safer and more effective application of this natural weak-acid repair cream in preventing post-radiotherapy ARD in breast cancer patients.
CONDITIONS
Official Title
Modulating the Skin Microbiome to Prevent Radiation Dermatitis in Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to less than 70 years with pathologically confirmed breast cancer
- TNM stage T1-3N1-3M0 or T3-4N0M0
- Underwent mastectomy with or without implant reconstruction
- Medically fit for adjuvant radiotherapy and able to tolerate side effects like fatigue, nausea, or vomiting
- No use of other skincare products during the study
- Voluntary participation with signed informed consent and agreement to follow study product use instructions
You will not qualify if you...
- History of prior radiotherapy
- Severe systemic diseases such as major heart, liver, or kidney problems; immunocompromising conditions including lymphoma, AIDS, or Wiskott-Aldrich syndrome
- History of other malignancies
- Skin reactions due to systemic therapies or active skin conditions in the treatment area
- Known allergy to the natural weak-acid repair cream or its ingredients
- Current participation in other clinical trials or participation within the past 3 months
- Poor compliance expected to prevent study completion
AI-Screening
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Trial Site Locations
Total: 1 location
1
Sun Yat-sen Memorial Hospital
Guangzhou, Guangdong, China
Actively Recruiting
Research Team
C
Chen Dr
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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