Bullseye ultrasound for lymphedema measurement - Clinical Trial

What is the Purpose of this Study?

We are doing this study to see if a new, hand-held, and non-invasive ultrasound device (called Bullseye) can detect lymphedema in people with known lymphedema.

What is the Condition Being Studied?

Lymphedema (Fluid in the Arm) after Breast Cancer

Who Can Participate in the Study?

Adults ages 18+ who:
- Have a history of breast cancer on one side
- Have lymphedema of any stage

For more information about who can be in this study, please contact the clinical trials office at (919) 668-3726.

Age Group
Adults

What is Involved?

If you choose to join the study, at your regular clinic visit you will:
- Have the usual volumetric (tape measure) lymphedema measurements of both your arms
- Have ultrasound measurements in the same places using the Bullseye study device
- Answer questionnaires

Some of the study questionnaires can be done online before or after your visit. You can review and complete a consent form to join the study during the study visit, or we can also email it to you before your visit.

You will only need to make this single visit to our clinic to complete the study.

Study Details

Full Title
A Pilot Study of Noninvasive Assessment of Lymphedema Among Breast Cancer Survivors
Principal Investigator
Radiation Oncologist
Protocol Number
IRB: PRO00109917
NCT: NCT05278871
Phase
Phase Pilot
ClinicalTrials.gov
Enrollment Status
Open for Enrollment
Participate
Contact the Duke Recruitment Innovation Center
MyResearchPartners@duke.edu
or
919-681-5698