Actively Recruiting
Topical Periplaneta Americana-Derived Meilian Fuxin Liquid for Radiation Dermatitis
Led by West China Hospital · Updated on 2026-03-25
60
Participants Needed
2
Research Sites
69 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate the efficacy and safety of topical Periplaneta americana-derived Meilian Fuxin Solution for the prevention of radiation dermatitis in patients undergoing radiotherapy.
CONDITIONS
Official Title
Topical Periplaneta Americana-Derived Meilian Fuxin Liquid for Radiation Dermatitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 80 years, any gender
- Confirmed diagnosis of head and neck cancer, including nasopharyngeal carcinoma, requiring radical or postoperative radiotherapy
- ECOG Performance Status score between 0 and 2
- Voluntary agreement to participate and signed informed consent
You will not qualify if you...
- History of prior radiotherapy to the target treatment area
- Presence of open wounds, infections, rash, psoriasis, or other skin conditions in the treatment area that affect assessment
- Having connective tissue diseases or other systemic skin disorders
- Known allergy to any component of Meilian Fuxin Solution
- Participation in other interventional clinical trials within the past 3 months or use of investigational drugs/devices
- Considered unsuitable for the study by the investigator
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Sichuan University West China Hospital, Chengdu, Sichuan
Chengdu, Sichuan, China, 610041
Actively Recruiting
2
Sichuan University West China Hospital
Chengdu, Sichuan, China
Actively Recruiting
Research Team
X
Xingchen Peng
CONTACT
R
Ruiwan Yuan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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