ConditionLymphedema Arm
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDharmais National Cancer Center Hospital
About this trial
This study aims to evaluate the effectiveness of the Lymphovenous Bypass (LVB) procedure compared to physiotherapy alone as secondary prevention of lymphedema in breast cancer patients undergoing axillary lymph node dissection.
Eligibility criteria
Qualifiers
Breast cancer patients aged ≥ 18 years with an ECOG score > 1
Breast cancer patients with post-axillary lymph node dissection diagnosed with stage 0 and I lymphedema.
Those who have never undergone lymphedema physiotherapy.
Disqualifiers
Patients with dermal backflow before axillary lymph node dissection (ALND).
Patients with breast cancer lymphedema who are unable to undergo a 24-month follow-up at Dharmais Cancer Hospital.
Patients with iodine allergy, severe asthma, decreased kidney function, pregnancy, or breastfeeding.
Trial design
Treatments tested in this trial
- Lymphovenous bypass (LVB)
Treatment groups
136 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov