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Screening for Edema and Breast Cancer-Related Lymphedema in Patients Undergoing Targeted Therapy for Breast Cancer

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

This a prospective, longitudinal study designed to track edema and Breast Cancer Related Lymphedema (BCRL) onset in breast cancer patients taking targeted therapy treatments for early and metastatic breast cancer. A Perometer and Sozo devise will be used to measure volume changes

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Subjects who are receiving treatment in the MGH Breast Cancer Center who are enrolled in a DF/HCC-regulated targeted therapy trial for the treatment of early or metastatic breast cancer or patients being treated with a targeted therapy that may alter their risk of developing edema or BCRL will be eligible.

• Subjects that will be eligible for the study include:

• Females between 18 and 80 years of age

• With a history of breast cancer

• 4 weeks or more post-surgery

• With or without edema

• Undergoing treatment with targeted therapy for early or metastatic disease.

Locations
United States
Massachusetts
Massachusetts General Hospital
RECRUITING
Boston
Contact Information
Primary
Alphonse G. Taghian, MD
ataghian@partners.org
617-643-1306
Time Frame
Start Date: 2018-12-13
Estimated Completion Date: 2026-09-30
Participants
Target number of participants: 261
Treatments
Target Therapy Drug-Stand Care
Screening procedures confirm participation in the research study.~* Participants limb volume is measured prior to treatment start date.~* Participant is provided informational brochure about risk of lymphedema and Lymphedema Screening Program Card.~* Perometer and SOZO measurements will be incorporated as a part of the follow-up visits throughout the course of their trial and for at least 6 months beyond their last dose of trial medication
Target Therapy-Early or Metastatic Breast Cancer
Screening procedures confirm participation in the research study.~* Participants limb volume is measured prior to treatment start date.~* Participant is provided informational brochure about risk of lymphedema and Lymphedema Screening Program Card.~* Perometer and SOZO measurements will be incorporated as a part of the follow-up visits throughout the course of their trial and for at least 6 months beyond their last dose of trial medication
Related Therapeutic Areas
Sponsors
Leads: Massachusetts General Hospital
Collaborators: Heinz Family Foundation

This content was sourced from clinicaltrials.gov