Breast Cancer Lymphedema

6

Review clinical trials related to Breast Cancer Lymphedema. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Screening For BCRL In Targeted Therapy For Breast Cancer

This a prospective, longitudinal study designed to track edema and Breast Cancer Related Lymphedema (BCRL) onset in breast cancer patients taking targeted therapy treatments for early and metastatic breast cancer. A Perometer and Sozo devise will be used to measure volume changes

Participants needed: 261
Trial details
Age: 18-80Biological sex: FemaleType: ObservationalSponsor: Massachusetts General HospitalUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Subjects who are receiving treatment in the MGH Breast Cancer Center who are enr... [+5]

Status: Not yet recruiting

Preoperative Indocyanine Green Lymphography and High-Frequency Ultrasound as Predictors of Lymphaticovenous Anastomosis Outcome in Post-Mastectomy Upper Limb Lymphedema

This study aims to evaluate the predictive value of preoperative indocyanine green (ICG) lymphography and high-frequency ultrasound in determining the outcomes of lymphaticovenous anastomosis (LVA) in patients with post-mastectomy upper limb lymphedema. Patients undergoing LVA surgery will undergo preoperative assessment using ICG lymphography and ultrasound mapping of lymphatic vessels and recipient veins. Surgical outcomes will be assessed clinically and functionally through limb circumference measurements, symptom improvement, and postoperative imaging findings. The study seeks to identify imaging predictors associated with successful LVA outcomes and improved postoperative recovery.

Participants needed: 30
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: May 29, 2026Locations: 1
Eligibility criteria

• Female patients aged 18 to 75 years. [+4]

Bilateral upper limb lymphedema. [+5]

Status: Recruiting

ILR to Prevent BRCL_MCC 23608

The goal of this clinical trial is to evaluate the effectiveness of Immediate Lymphatic Reconstruction (ILR) in preventing breast cancer-related lymphedema (BCRL) in high-risk patients. It will also assess the safety and quality of life outcomes associated with the procedure. The main questions it aims to answer are: Does ILR reduce the incidence of BCRL in patients undergoing axillary lymph node dissection (ALND)? What are the patient-reported outcomes and quality of life differences between those who receive ILR and those who do not? Participants will be identified as high-risk for developing BCRL through a multidisciplinary tumor board and referred to a specialized clinic for further evaluation. High-risk patients will undergo a series of screening tests, including bioimpedance spectroscopy (BIS), circumferential limb measurements, and infrared 3D perometry. Participants will be randomly assigned to one of two groups: Intervention Group (Study Arm A): Undergo ILR during ALND surgery, where preserved lymphatic channels are connected to nearby veins to prevent lymphedema. Control Group (Study Arm B): Will not receive ILR, but efforts will be made to preserve lymphatic channels during surgery. Patients will be blinded to their group assignment. Post-surgery, all participants will receive education from a certified lymphatic physical therapist. At the 2-week postoperative visit, participants will be further randomized into two postoperative monitoring protocols: BCRL Clinical Pathway: Patients will have regular follow-up visits every three months for two years, including repeat BIS, limb measurements, perometry, and quality of life questionnaires (LYMQOL and ULL-27). Standard of Care: Patients will be monitored only if they experience BCRL symptoms or after two years from ALND. The study will compare the outcomes of both groups, with a focus on the incidence of BCRL and patient quality of life, and will benchmark these results against published literature on breast cancer patients.

Participants needed: 98
Trial details
Age: 18-75Biological sex: FemaleType: InterventionalSponsor: University of South FloridaUpdated: Apr 30, 2026Locations: 3
Eligibility criteria

Patients consenting for unilateral ALND [prior history of sentinel lymph node bi... [+3]

• Male breast cancer patients [+13]

Status: Not yet recruiting

Effects of Combined Upper Extremity Exercise and Pneumatic Compression Therapy on Breast Cancer-Related Lymphedema

Breast cancer is one of the most common cancers among women worldwide. With advances in treatment, survival rates have steadily increased; however, postoperative complications continue to affect patients' quality of life, with upper extremity lymphedema being among the most prevalent. Breast cancer related lymphedema (BCRL) can result in arm swelling, pain, restricted mobility, and psychological distress, all of which negatively impact daily functioning and social partici pation . Previous studies have demonstrated that regular and moderate upper extremity exercise does not exacerbate lymphedema; instead, it may improve shoulder mobility, muscular strength, and contribute to edema control. In addition, therapeutic modalities such as pneumatic compression pumps and manual lymphatic drainage have been proven effective in reducing swelling and enhancing patient comfort . Recent systema tic reviews further support the beneficial effects of exercise interventions on upper limb function and quality of life in breast cancer survivors. Therefore, combining upper extremity exercise with pneumatic compression therapy may re present a promising integrative intervention to improve lymphedema and related functional limitations. This study aims to investigate the effects of such a combined approach on breast cancer patients with lymphedema by comparing outcomes across multiple ti me points, including arm circumference measurements, shoulder range of motion, upper extremity function (DASH), and quality of life (FACT B), with the goal of establishing a more comprehensive rehabilitation model.

Participants needed: 20
Trial details
Age: 20-70Biological sex: FemaleType: InterventionalSponsor: Far Eastern Memorial HospitalUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Female breast cancer patients aged 20-70 years [+3]

Breast cancer with a tendency for recurrence or metastasis [+5]

Status: Recruiting

LLLT for BCRL: a Randomized, Placebo-controlled Study

This study is conducted to compare between efficacy of large and small area of low-level laser therapy (LLLT) in treatment of post mastectomy lymphedema. The change of severity of BCRL will be measured by the difference of circumference and skin thickness, detected by ultrasound. The influence on clinical symptoms, such as pain, shoulder mobility and hand function, are also investigated in the study.

Participants needed: 54
Trial details
Age: 20+Biological sex: FemaleType: InterventionalSponsor: National Taiwan University HospitalUpdated: Oct 18, 2024Locations: 1
Eligibility criteria

Female subjects, 20 years age or older, suffered from unilateral breast cancer w... [+3]

Metastatic cancer(stage IV) [+9]

Status: Not yet recruiting

Lymphatic Response to Resistance Exercise in Breast Cancer Survivors

The objective of this study is 1) to study the acute and chronic effect of resistance therapeutic physical exercise (RTPE) in the prevention of breast cancer-related lymphedema (BCRL) in breast cancer survivors at risk using variables related to the lymphatic response; 2) Study the possible relationship between changes in body composition at a local and regional level and volume changes produced by RTPE in patients at risk of suffering from BCRL.

Participants needed: 170
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of MalagaUpdated: Nov 2, 2023Locations: 1
Eligibility criteria

Women diagnosed with breast cancer [+8]

Women already diagnosed with LACM in stage I, II or III according to the ISL or... [+8]