Breast Cancer Clinical Trial

Topical Use of Difinsa53â„¢ to Prevent Radiation Dermatitis

Summary

Phase II trial of the silibin containing cream, Difinsa53 to determine efficacy in delaying, ameliorating, or preventing radiation dermatitis in patients with breast cancer undergoing whole breast radiation.

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Full Description

The proposed study seeks to evaluate the efficacy of DIFINISA53â„¢, a safe silibin-based skin cream, on preventing radiation dermatitis (RD) when compared to an over the counter ointment, Aquaphor, in women undergoing radiation therapy for breast cancer following lumpectomy or mastectomy surgery. Presently there is no known fully effective topical protectant from RD and there is no consensus among radiation oncologists on how best to treat RD. This study seeks to identify a more effective option for patients receiving radiation therapy. Each participant will apply the DIFINISA53â„¢ cream to one area of the treated skin and Aquaphor to another area of treated skin. Skin reactions will be evaluated using medical professional assessment, participant assessment, and photographic assessment by a third party.

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Eligibility Criteria

Inclusion Criteria:

Female patients 18 years and older
Pathologic diagnosis of breast cancer requiring radiation therapy to whole breast
Able to apply lotion to treatment area at least twice daily during radiation course
All surgical sites healed
No evidence of infection
No history of sensitivity to any component in Aquaphor or Difensa53

Exclusion Criteria:

Prior history of radiation therapy (RT) to that site
Known dermatologic conditions affecting skin in radiation port
Concurrent chemotherapy
Skin infection in radiation port
History of sensitivity to Aquaphor or Difensa53 component

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

13

Study ID:

NCT02534129

Recruitment Status:

Terminated

Sponsor:

ProTechSure Scientific, Inc.

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There is 1 Location for this study

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Poudre Valley Health System
Fort Collins Colorado, 80528, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

13

Study ID:

NCT02534129

Recruitment Status:

Terminated

Sponsor:


ProTechSure Scientific, Inc.

How clear is this clinincal trial information?

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