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Lymphedema clinical trials

View clinical trials related to Lymphedema.

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NCT ID: NCT03584633 Enrolling by invitation - Lymphedema Clinical Trials

Effect of Exercise on Indocyanine Green (ICG) Lymphography Imaging

Start date: April 15, 2019
Phase: Phase 4
Study type: Interventional

Indocyanine Green (ICG) lymphography is a relatively new imaging technique that allows for quick visualization of superficial lymph flow in real-time, without radiation exposure. This imaging is useful for diagnosing and assessing lymphedema. ICG lymphography has a higher sensitivity and specificity than lymphoscintigraphy, the current gold standard imaging device for lymphedema. ICG lymphography precisely and reliably diagnoses, tracks, and stages lymphedema severity, ranging from subclinical or early lymphedema to more advanced cases. The ICG contrast dye used to visualize the lymphatic system takes approximately six hours to plateau. Therefore, patients must wait six hours between their initial and delayed scans. The purpose of this study is to determine if exercising on a Nu-step device between ICG initial and delayed scans would shorten the period of time a patient had to spend at the hospital on the day of their ICG lymphography. The general procedures for this involve (after selecting subjects, consenting subjects, educating the subject on the protocol, along with other appropriate measures): - Taking baseline vitals (HR & SpO2) and limb circumference measurements - 5-minute period of time to acquaint subject with the exercise equipment (Nu-Step) at any level of exertion - injection of contrast agent to allow for visualization of the superficial lymphatic system by a qualified nurse - Initial scan - A 5-minute period of exercise at "moderate" level of exercise (This correlates to the rating of perceived exertion levels of 12-13; All exercise periods should be at this level and will be monitored by a provider) - Second scan & vitals - 5-minute period of exercise - Third scan & vitals o Continue 5-minute exercise period followed by scan & vitals until disease pattern emerges * Exercise for 5 minutes then scan and vitals until images reach steady state for two consecutive scans - Final vitals (HR & SpO2) * Repeat scan every 1 hour until the normal 6 hour scan to monitor for further changes in lymphatic pattern. - Exit survey

NCT ID: NCT02550951 Enrolling by invitation - Lymphedema Clinical Trials

Utility of MR Lymphangiography in Postoperative Follow-up of Lymphedema: Comparison With Lymphoscintigraphy

Start date: October 2014
Phase: N/A
Study type: Interventional

Its usefulness in implementing magnetic resonance angiography for postoperative follow-up of lymph lymphedema should try to evaluate and compare lymphoscintigraphy.

NCT ID: NCT02375165 Enrolling by invitation - Lymphedema Clinical Trials

Biomarkers for the Detection of Lymphatic Insufficiency

Biomarkers
Start date: September 2009
Phase:
Study type: Observational

Acquired lymphedema is a disease that causes chronic swelling of the limb(s). It is frequently under-recognized or misdiagnosed. This study is designed to lead to the development of an accurate, noninvasive, blood test to allow testing for lymphedema. This approach is particularly useful to investigate relative responses to treatment interventions.

NCT ID: NCT01273909 Enrolling by invitation - Breast Cancer Clinical Trials

Outcomes After Perforator Flap Reconstruction for Breast Reconstruction and/or Lymphedema Treatment

Start date: July 2010
Phase: N/A
Study type: Observational

The goal of this prospective, observational study is to investigate the clinical, psychosocial, and patient satisfaction outcomes of patients who undergo perforator flap reconstruction for breast reconstruction and/or vascularized lymph node transfer (VLNTx) for the treatment of lymphedema. The investigators hypothesize that (1) perforator flap breast reconstruction will result in excellent clinical, psychosocial, and patient satisfaction outcomes compared to non-perforator flap breast reconstruction; (2) perforator flap breast reconstruction is associated with less persistent postsurgical pain than other forms of breast reconstruction, even after controlling for major cofactors, such as the extent of auxiliary lymph node dissection and the use of radiation therapy; (3) perforator flap reconstruction for the treatment of Lymphedema (i.e., VLNTx ) will result in the reduction of symptoms and complications of lymphedema.

NCT ID: NCT00833599 Enrolling by invitation - Lymphedema Clinical Trials

Imaging Lymphatic Function in Normal Subjects and in Persons With Lymphatic Disorders

Start date: January 2009
Phase:
Study type: Observational

The purpose of this study is to demonstrate the feasibility of near-infrared fluorescence imaging in subjects with acquired or hereditary lymphedema, in subjects with lipidema and other lymphovascular disorders and in normal health subjects; in order to attempt to correlate imaging phenotype(s) with genotype(s).