Bullseye ultrasound for lymphedema measurement
What is the Purpose of this Study?
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.
- 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.
What is the Condition Being Studied?
Lymphedema (Fluid in the Arm) after Breast Cancer
Who Can Participate in this 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
Participating Institutions
What is Involved?
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.
Study Details
Full Title
A Pilot Study of Noninvasive Assessment of Lymphedema Among Breast Cancer Survivors
Principal Investigator
Protocol Number
IRB:
PRO00109917
NCT:
NCT05278871
ClinicalTrials.gov
View on ClinicalTrials.gov