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Spots Global Cancer Trial Database for PORTAL: Patient-reported Outcomes After Routine Treatment of Atypical Lesions

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: PORTAL: Patient-reported Outcomes After Routine Treatment of Atypical Lesions

Official Title: PORTAL: Patient-reported Outcomes After Routine Treatment of Atypical Lesions

Study ID: NCT03070236

Conditions

Breast Cancer

Interventions

Survey

Study Description

Brief Summary: This research study is evaluating how patients feel physically and emotionally after a prior breast biopsy for specific breast conditions (including atypical lesions such as atypical ductal hyperplasia (ADH), atypical lobular hyperplasia (ALH), lobular carcinoma in situ (LCIS), and/or ductal carcinoma in situ (DCIS))

Detailed Description: The goal of this research is to better understand the experience of women who have been diagnosed with certain breast conditions to enable women (and their doctors) to make informed decisions about their care.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Massachusetts General Hospital, Boston, Massachusetts, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Newton-Wellesley Hospital, Newton, Massachusetts, United States

Dana-Farber/Brigham and Women's Cancer Center in clinical affiliation with South Shore Hospital, Weymouth, Massachusetts, United States

Duke University Medical Center, Durham, North Carolina, United States

MD Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Ann H. Partridge, MD, MPH

Affiliation: Dana-Farber Cancer Institute

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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