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Lymphedema clinical trials

View clinical trials related to Lymphedema.

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NCT ID: NCT04390685 Active, not recruiting - Lymphedema Clinical Trials

Prevention of Breast Cancer-related Lymphedma With Tacrolimus

BCRL-TACRO
Start date: February 26, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Breast cancer-related lymphedema is one of the most common and feared consequences of breast cancer treatment. Tacrolimus ointment may prevent lymphedema by inhibition of CD4+T cells.

NCT ID: NCT04241341 Active, not recruiting - Clinical trials for Breast Cancer Lymphedema

Does Immediate Lymphatic Reconstruction Decrease the Risk of Lymphedema After Axillary Lymph Node Dissection

Start date: January 22, 2020
Phase: Phase 3
Study type: Interventional

The researchers are doing this study to see if having immediate lymphatic reconstruction after axillary lymph node dissection (ALND) can decrease the development of lymphedema, a side effect of ALND. Other purposes of the study include: Comparing the approach of immediate lymphatic reconstruction after ALND with the approach of ALND alone Looking at whether having immediate lymphatic reconstruction after ALND improves a person's quality of life Seeing if adding standard of care radiation therapy to either study approach (immediate lymphatic reconstruction after ALND or ALND alone) has an effect on development of lymphedema

NCT ID: NCT03927027 Active, not recruiting - Clinical trials for Breast Cancer Stage II

Axillary Reverse Mapping in Preventing Lymphedema in Patients With Breast Cancer Undergoing Axillary Lymph Node Dissection

Start date: July 29, 2019
Phase: Phase 3
Study type: Interventional

This phase III trial studies how well axillary reverse mapping works in preventing lymphedema in patients with breast cancer undergoing axillary lymph node dissection. Axillary reverse mapping may help to preserve the lymph node drainage system around the breast so as to prevent lymphedema after surgery.

NCT ID: NCT03760744 Active, not recruiting - Clinical trials for Secondary Lymphedema

Imaging Biomarkers of Lymphatic Dysfunction

Start date: January 23, 2019
Phase: N/A
Study type: Interventional

Persons with secondary arm and/or upper quadrant lymphedema following cancer therapies commonly are prescribed complete decongestive therapy as a course of management of their lymphedema. The investigators will perform a repeated-measures cross-over trial to test the hypothesis that mobilization of protein enriched hardened tissue using graded negative pressure therapy in conjunction with complete decongestive therapy (CDT) is more effective to standard CDT alone for secondary lymphedema management.

NCT ID: NCT03658967 Active, not recruiting - Clinical trials for Secondary Lymphedema

Clinical Study With Lymfactin® in the Treatment of Patients With Secondary Lymphedema (AdeLE)

AdeLE
Start date: June 7, 2018
Phase: Phase 2
Study type: Interventional

This study evaluates the efficacy of Lymfactin® in patients with secondary lymphedema associated with the treatment of breast cancer by comparing the effects of active study treatment Lymfactin® to placebo. The study product will be administered in combination with a surgical lymph node transfer operation. In addition, the safety and tolerability of the Lymfactin® treatment will be evaluated.

NCT ID: NCT03428581 Active, not recruiting - Breast Cancer Clinical Trials

Preventing Lymphedema in Axillary Lymph Node Dissection

Start date: April 10, 2018
Phase: N/A
Study type: Interventional

The researchers are trying to answer if axillary reverse mapping (ARM) with lympho-venous bypass (LVB) in patients undergoing an axillary lymph node dissection reduces the rate and severity of post-operative lymphedema of the arm.

NCT ID: NCT03379805 Active, not recruiting - Clinical trials for Univentricular Heart

Lymphatic Function in Patients With a Fontan-Kreutzer Circulation

Start date: April 25, 2014
Phase: N/A
Study type: Observational

The lymphatics regulate the interstitial fluid by removing excessive fluid. It represents an extremely important step in the prevention of edema. The Fontan-Kreutzer procedure has revolutionized the treatment of univentricular hearts. However, it is associated with severe complications such as protein-losing enteropathy (PLE) and peripheral edema that may involve the lymphatic circulation. Our hypothesis is that patients with a univentricular circulation have a reduced functionality of the lymphatic vasculature, which predisposes them to developing complications such as edema and PLE. The functional state of lymphatics is investigated using near infrared fluorescence imaging, NIRF. The anatomy is described using non-contrast MRI and the capillary filtration rate is measured using plethysmography.

NCT ID: NCT03292198 Active, not recruiting - Clinical trials for Breast Cancer-related Subclinical Lymphedema

Subclinical Lymphedema Treatment Study

SLT
Start date: April 1, 2018
Phase: N/A
Study type: Interventional

Primary Objective - To compare the effectiveness of 2 treatment protocols for patients with breast cancer-related subclinical lymphedema identified through bioimpedance spectroscopy, L-dex scores Secondary Objectives - To determine the necessary duration of intervention to reverse L-dex scores back to a normal range in patients with breast cancer-related subclinical lymphedema - To determine the time elapsed post-surgically to the development of subclinical lymphedema identified by bioimpedance spectroscopy, L-dex scores - To identify risk factors for the development of subclinical lymphedema in patients with breast cancer - To identify factors associated with the progression to clinical lymphedema following treatment of subclinical lymphedema as identified by bioimpedance spectroscopy, L-dex scores Women with breast cancer diagnoses and planned axillary lymph node procedures will receive pre-operative screening of arm volume with bioimpedance, which will capture baseline measurements. Then, subjects will undergo periodic screenings for the first 3 years following surgery. If a significant change in volume compared to baseline is detected with bioimpedance, subjects will be randomized to 1 of 2 treatment groups. The outcomes of 2 treatment protocols will be compared. Additionally, subjects will be screened each week during their treatment interventions to determine the necessary quantity of intervention before L-dex scores normalize.

NCT ID: NCT03127995 Active, not recruiting - Clinical trials for Breast Cancer Female

Hypofractionated vs Standard Radiotherapy in Breast Cancer With an Indication for Regional Lymph Node Irradiation About Lymphedema Occurrence

HYPOG-01
Start date: September 2016
Phase: N/A
Study type: Interventional

The standard treatment of localized breast cancers consists of surgical removal of the tumor at the breast or removal of the entire breast and lymph nodes (sentinel lymph node and / or axillary dissection) with or without chemotherapy followed by radiotherapy on the breast or thoracic wall and the lymph node areas from 5 to 6.5 weeks. Shorter radiotherapy treatments over 3 weeks for breast cancer without lymph node involvement have been equally effective and have no more side effects in several clinical trials involving several thousand patients. This called hypofractionated radiotherapy has become a standard for breast cancers in the absence of lymph node involvement in postmenopausal women. The objective of the HypoG01 trial is to evaluate hypofractionated radiotherapy in women who require radiotherapy in the breast or chest wall and lymph node areas by comparing standard over 5 to 6.5 weeks and hypofractionated irradiation over 3 weeks analyzing the possible side effects and in particular the risk of lymphedema (swelling of the arm on the side treated) and the effectiveness of these treatments

NCT ID: NCT02992782 Active, not recruiting - Lymphedema Clinical Trials

Decongestive Exercise and Compression for Breast Cancer Related Lymphedema Management

DREAM
Start date: June 1, 2017
Phase: N/A
Study type: Interventional

Women who have undergone breast cancer surgery may develop swelling of the arm on the side the breast cancer occurred. If the swelling becomes chronic it is called lymphedema. This study will examine the effect of a 12-week decongestive progressive resistance exercise with advanced compression on breast cancer related lymphedema. Our objective is to determine if breast cancer survivors are willing and able to wear advanced compression while exercising and if the combination will help to reduce their lymphedema. Twenty-four breast cancer survivors from Edmonton, Alberta will be enrolled in the one-year long study.