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Dilute Sodium Hypochlorite solution for Radiation Skin Damage
N/A
Waitlist Available
Led By Amy Paller, MD
Research Sponsored by Northwestern University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 weeks
Awards & highlights
Study Summary
Utilizing Topical Sodium Hypochlorite to Ameliorate Radiation Dermatitis
Eligible Conditions
- Radiation Skin Damage
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Compliance with compress application
Improvement in patient reported outcome measures
Occurrence of adverse events from compress application
Trial Design
1Treatment groups
Experimental Treatment
Group I: Treatment with Dilute Sodium Hypochlorite solutionExperimental Treatment1 Intervention
Subjects will be treated with the dilute bleach compresses daily (Monday through Friday) for the first 3 weeks of therapy. The bleach solution will be prepared and compresses applied for a 20 minute duration prior to radiation therapy. The compress can be applied within an hour of radiation therapy. Subjects will apply Aquaphor® ointment twice a day, once immediately after the radiation treatment and once in the evening. On days the experimental subjects do not receive radiation therapy, they will continue to moisturize their skin twice a day (AM and PM) with Aquaphor® ointment.
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Who is running the clinical trial?
Northwestern UniversityLead Sponsor
1,586 Previous Clinical Trials
917,245 Total Patients Enrolled
Amy Paller, MDPrincipal Investigator - Department of Dermatology, Chair
Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern Memorial Hospital
Stanford University School Of Medicine (Medical School)
Northwestern Mem Hospital (Residency)
17 Previous Clinical Trials
2,676 Total Patients Enrolled
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