None listed
Conditions
Interventions
Medical Device : During the lymphoscintigraphy test, 30 minutes after radioisotope injection, cuffs will be worn on both upper extremities, and pressure pumps (UAM-12000NB) will be operated to sequent
Sponsors
Seoul National University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Breast cancer patients who visited for lymphedema treatment 2. Those who can read and fill out questionnaires 3. Adult men and women over 20 years old 4. Those who agreed to participate in the study and follow-up observation
Exclusion criteria
Exclusion criteria: 1. Patients with poor general condition so that it is difficult to perform the test 2. People with serious psychiatric problems 3. Employees or students within the research institute that are judged to be difficult to voluntarily participate 4. Others In addition to the above items, if the clinical trial researcher is judged to be inadequate or difficult to respond to the survey
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The number of successfully treated patients (volume reduction by more than 15%) in the experimental group and the control group according to the imaging finding | — |
Secondary
| Measure | Time frame |
|---|---|
| Average volume reduction rate after treatment compared to baseline in the experimental group;Comparison of average of edema reduction according to other imaging findings;QOL score using EORTC after treatment against baseline | — |
Countries
Korea, Republic of
Contacts
Public Contactjimin lee
Seoul National University Hospital
Outcome results
None listed