Erythema Clinical Trial
Official title:
Evaluation of a Novel Amino Acid Based Moisturizing Cream as Part of the Daily Standard Skincare Regimen Recommended During Radiation Therapy
The goal of this clinical study is to evaluate a novel amino acid based moisturizing cream as part of the daily standard skincare regimen recommended during radiation therapy. The main aim of this study is to assess if the investigational product can improve skin redness associated with radiation therapy. Participants will apply a moisturizer daily during the course of their prescribed radiation therapy for breast cancer. Researchers will compare against the standard of care.
Status | Not yet recruiting |
Enrollment | 70 |
Est. completion date | March 18, 2024 |
Est. primary completion date | March 18, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Provision of signed and dated informed consent form. - Aged over 18 years old. - Has been diagnosed with breast cancer and prescribed radiotherapy as a part of their cancer treatment. - Planned radiotherapy, as prescribed by the oncologist, is expected to provide a total radiation dose of up to 60 gray within the first 4 weeks of treatment. - Be able to adhere to proposed daily wound/site care as proposed by the protocol in line with the AADs recommendations. Exclusion Criteria: - Pre-existing skin conditions which in the opinion of the investigator could impact on the integrity of the study or compromise the safety of the patient (i.e., active eczema, psoriasis, or an open wound over the planned site of radiation). - Have a concurrent medical condition or poor functional baseline which in the opinion of the investigator would make them unsuitable or able to fully comply with the study protocol. - Are pregnant or actively breast feeding. - Known allergic reactions to ingredients of the Investigational Product or the Standard of Care. |
Country | Name | City | State |
---|---|---|---|
United States | Advocate Radiation Oncology | Fort Myers | Florida |
Lead Sponsor | Collaborator |
---|---|
Entrinsic Bioscience Inc. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduction in Erythema | Evaluation of skin redness (both severity and size) with ScarletRed technology | Up to 12 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
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