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Spots Global Cancer Trial Database for Curcumin for the Prevention of Radiation-induced Dermatitis in Breast Cancer Patients

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Curcumin for the Prevention of Radiation-induced Dermatitis in Breast Cancer Patients

Official Title: Curcumin for the Prevention of Radiation-induced Dermatitis in Breast Cancer Patients

Study ID: NCT01042938

Conditions

Breast Cancer

Study Description

Brief Summary: Ionizing radiation is a toxic agent and widely accepted form of treatment for various types of cancer. Despite advances in medical technology, radiation therapy still causes severe early and late skin effects. Radiation-induced dermatitis occurs in approximately 80% of patients. Important consequences of radiation-induced dermatitis include impairment of the quality of a patient's life due to pain and premature interruption of radiation treatment, which in turn, may be impair good local control of disease. The biological pathways responsible for acute radiation-induced dermatitis remain unclear. Currently, there is no standard treatment for the prevention of radiation-induced dermatitis with demonstrated effectiveness. The aim of this randomized, double-blind, placebo-controlled pilot study is to assess the effectiveness of curcumin for the prevention of acute radiation-induced dermatitis during postoperative radiotherapy for breast cancer. We hypothesize that curcumin, a natural phenolic compound found in both turmeric and curry powders, can prevent or alleviate radiation-induced skin reactions in breast cancer patients receiving radiotherapy.

Detailed Description: Specifically, this clinical pilot study will develop data necessary to calculate a sample size for a larger study to be conducted through the National Cancer Institute (NCI) Community Clinical Oncology Program (CCOP) mechanism. Specifically, this pilot project will investigate: 1) if curcumin can prevent or alleviate radiation-induced skin reactions in cancer patients receiving radiotherapy and 2) if skin pigmentation, as well as pain and psychophysiological factors, can predict the severity of radiation-induced dermatitis. Potential future research studies may be conducted to identify the biological mechanisms involved in radiation-induced dermatitis and the radioprotective function of curcumin.

Eligibility

Minimum Age: 21 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

University of Rochester Medical Center & Wilmot Cancer Center, Rochester, New York, United States

Contact Details

Name: Julie L Ryan, PhD, MPH

Affiliation: University of Rochester Medical Center & Wilmot Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Name: Julie L Ryan, PhD, MPH

Affiliation: University of Rochester Medical Center & Wilmot Cancer Center

Role: STUDY_CHAIR

Name: Alice P Pentland, MD

Affiliation: University of Rochester Medical Center & Wilmot Cancer Center

Role: STUDY_CHAIR

Name: Marilyn Ling, MD

Affiliation: University of Rochester Medical Center & Wilmot Cancer Center

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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