Comparing Level 1 Compression Sleeves With Routine Care in Preventing Breast Cancer-related Arm Lymphedema
Breast Cancer-related Arm Lymphedema
About this trial
This is an interventional treatment trial for Breast Cancer-related Arm Lymphedema focused on measuring breast cancer-related arm lymphedema, bioimpedance spectroscopy, Limb circumference measurement
Eligibility Criteria
Inclusion Criteria: Patients aged 18 to 70 years old Breast cancer, unilateral,Patients undergoing axillary lymph node dissection Patients voluntarily joined the study and signed informed consent Exclusion Criteria: arm swelling preoperatively, as assessed by bioimpedance spectroscopy (BIS) or Limb circumference measurement any condition that hindered them from wearing a compression sleeve Patients with upper limb dysfunction before surgery, including shoulder and elbow joint mobility disorders Patients with mental disorders, senile dementia, and cognitive impairments,were not able to complete a questionnaire independently Patients with bilateral breast cancer, recurrence, or metastasis to other organs.
Sites / Locations
- Henan Cancer Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Prophylactic compression sleeves group
routine care group
The intervention group will wear compression sleeves for upper limbs with a pressure level of 1 (15-20mmHg) during the day for 12 months.
The routine care group will proceed as an observation and receive standard lymphedema education during the clinical trial.