Prospective Assessments Following Immediate Lymphatic Reconstruction

Recruiting Observational Study
Lymphatic Reconstruction
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
100 (estimated)
Sponsor
University of Chicago · Other
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About This Trial
Immediate lymphatic reconstruction (ILR) is a novel surgical approach performed at the time of initial lymph node dissection with the goal of preventing lymphedema.(Chang et al. 2020) It involves the identification of lymphatic channels that are transected after lymph node dissection and microsurgical anastomosis of one or more lymphatic channel with a local recipient vein to re-direct upper extre…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: potential candidates for ILR based on possible nodal involvement assessed preoperatively. Exclusion Criteria: * Individuals who are not eligible for ILR based on possible nodal involvement assessed preoperatively.
Contacts

Summer Hanson, MD, PhD, FACS

(773) 702-6302

sehanson@bsd.uchicago.edu

CONTACT