PREVENT: PeRomEter Visualization to ENd Treatment-related Lymphedema
Running, not enrolling · Not applicable
Conditions studied: Lymphedema
In brief
This research study is to learn about breast cancer patients' opinions about screening for lymphedema (a side effect of breast cancer treatment in which the arm can become heavy, painful, and/or swollen) and their satisfaction with the lymphedema screening program.
Key facts
- Study ID
- NCT05056207
- Run by
- M.D. Anderson Cancer Center
- People needed
- 260
- Starts
- 2017-11-17
- Expected to finish
- 2026-11-17
- Last updated by the study team
- 2026-03-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- a Cohort A:
- Breast cancer patients with a baseline (preoperative perometer measurements) who have undergone axillary lymph node dissection
- English speaker
- Patients who participate in Cohort A will be eligible for enrollment in Cohort
- b Cohort I:
- Breast cancer patients who have undergone axillary lymph node dissection who have a clinic visit in the Nellie B. Connally Breast Center approximately 12 months (+/- 4 months) following axillary lymph node dissection
- English speaker
- c Cohort II:
- Breast cancer patients who have undergone axillary lymph node dissection who are having a follow-up visit in the Nellie B. Connally Breast Center within 0-6 months following surgery who intend to continue follow-up care at MD Anderson
- English speaker
You may not qualify if…
- Inability to complete a self-administered questionnaire
Where it is running
- M D Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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